|
ENST00000423275.6:c.*594C>G
|
ENSP00000401088.1:n.*594C>G
|
|
|
ENST00000432427.3:c.249C>G
|
|
|
|
ENST00000465826.6:n.520C>G
|
|
|
|
ENST00000491290.2:n.1306C>G
|
|
|
|
ENST00000684903.1:c.*606C>G
|
ENSP00000508612.1:n.*606C>G
|
|
|
ENST00000685348.1:c.*606C>G
|
ENSP00000510285.1:n.*606C>G
|
|
|
ENST00000685437.1:c.830C>G
|
ENSP00000508794.1:p.Thr277Ser
|
|
|
ENST00000685438.1:n.693C>G
|
|
|
|
ENST00000685653.1:c.929C>G
|
ENSP00000509968.1:p.Thr310Ser
|
|
|
ENST00000685738.1:c.929C>G
|
ENSP00000510156.1:p.Thr310Ser
|
|
|
ENST00000686409.1:n.1637C>G
|
|
|
|
ENST00000686455.1:n.1292C>G
|
|
|
|
ENST00000686479.1:n.1300C>G
|
|
|
|
ENST00000686762.1:c.929C>G
|
ENSP00000509767.1:p.Thr310Ser
|
|
|
ENST00000687257.1:n.1165C>G
|
|
|
|
ENST00000687326.1:c.929C>G
|
ENSP00000509665.1:p.Thr310Ser
|
|
|
ENST00000687486.1:c.182+175C>G
|
|
|
|
ENST00000687505.1:n.1047C>G
|
|
|
|
ENST00000687923.1:c.830C>G
|
ENSP00000510255.1:p.Thr277Ser
|
|
|
ENST00000687940.1:n.1306C>G
|
|
|
|
ENST00000688269.1:n.1525C>G
|
|
|
|
ENST00000688326.1:c.249C>G
|
|
|
|
ENST00000688444.1:n.1255C>G
|
|
|
|
ENST00000688543.1:c.830C>G
|
ENSP00000509612.1:p.Thr277Ser
|
|
|
ENST00000688625.1:c.*507C>G
|
ENSP00000509522.1:n.*507C>G
|
|
|
ENST00000688803.1:n.1160C>G
|
|
|
|
ENST00000689097.1:c.*606C>G
|
ENSP00000509756.1:n.*606C>G
|
|
|
ENST00000689389.1:c.929C>G
|
ENSP00000510213.1:p.Thr310Ser
|
|
|
ENST00000689418.1:c.*606C>G
|
ENSP00000509467.1:n.*606C>G
|
|
|
ENST00000689481.1:c.*606C>G
|
ENSP00000510248.1:n.*606C>G
|
|
|
ENST00000689540.1:n.1079C>G
|
|
|
|
ENST00000689876.1:c.929C>G
|
ENSP00000508535.1:p.Thr310Ser
|
|
|
ENST00000689914.1:c.929C>G
|
ENSP00000509847.1:p.Thr310Ser
|
|
|
ENST00000690397.1:c.818C>G
|
ENSP00000508730.1:p.Thr273Ser
|
|
|
ENST00000690460.1:c.917C>G
|
ENSP00000509106.1:p.Thr306Ser
|
|
|
ENST00000690625.1:n.1232C>G
|
|
|
|
ENST00000691268.1:c.356C>G
|
|
|
|
ENST00000691396.1:c.*722C>G
|
ENSP00000510712.1:n.*722C>G
|
|
|
ENST00000691724.1:c.929C>G
|
ENSP00000509255.1:p.Thr310Ser
|
|
|
ENST00000691779.1:c.*507C>G
|
ENSP00000508592.1:n.*507C>G
|
|
|
ENST00000691899.1:c.929C>G
|
ENSP00000508763.1:p.Thr310Ser
|
|
|
ENST00000692069.1:n.1152C>G
|
|
|
|
ENST00000692093.1:c.830C>G
|
ENSP00000509669.1:p.Thr277Ser
|
|
|
ENST00000692311.1:n.1410C>G
|
|
|
|
ENST00000692558.1:n.1294C>G
|
|
|
|
ENST00000692773.1:c.*666C>G
|
ENSP00000509055.1:n.*666C>G
|
|
|
ENST00000692830.1:c.*674C>G
|
ENSP00000509461.1:n.*674C>G
|
|
|
ENST00000693069.1:c.830C>G
|
ENSP00000510072.1:p.Thr277Ser
|
|
|
ENST00000693312.1:c.704C>G
|
ENSP00000508686.1:p.Thr235Ser
|
|
|
ENST00000693664.1:c.929C>G
|
ENSP00000509614.1:p.Thr310Ser
|
|
|
ENST00000693705.1:c.*606C>G
|
ENSP00000510697.1:n.*606C>G
|
|
|
ENST00000251849.9:c.929C>G
MANE Select
|
ENSP00000251849.4:p.Thr310Ser
|
|
|
ENST00000442415.7:c.989C>G
|
ENSP00000401888.2:p.Thr330Ser
|
|
|
ENST00000251849.8:c.929C>G
|
ENSP00000251849.4:p.Thr310Ser
|
|
|
ENST00000423275.5:c.*606C>G
|
ENSP00000401088.1:n.*606C>G
|
|
|
ENST00000432427.2:c.566C>G
|
ENSP00000398591.2:p.Thr189Ser
|
|
|
ENST00000442415.6:c.989C>G
|
ENSP00000401888.2:p.Thr330Ser
|
|
|
ENST00000465826.5:n.173C>G
|
|
|
|
ENST00000491290.1:n.558C>G
|
|
|
|
NM_002880.3:c.929C>G , LRG_413t1:c.929C>G
|
NP_002871.1:p.Thr310Ser
|
|
|
XM_005265355.1:c.929C>G
|
XP_005265412.1:p.Thr310Ser
|
|
|
XM_005265357.1:c.830C>G
|
XP_005265414.1:p.Thr277Ser
|
|
|
XM_005265358.3:c.686C>G
|
XP_005265415.1:p.Thr229Ser
|
|
|
XM_005265359.3:c.587C>G
|
XP_005265416.1:p.Thr196Ser
|
|
|
XM_005265360.1:c.929C>G
|
XP_005265417.1:p.Thr310Ser
|
|
|
XM_011533974.1:c.929C>G
|
XP_011532276.1:p.Thr310Ser
|
|
|
XM_011533975.1:c.686C>G
|
XP_011532277.1:p.Thr229Ser
|
|
|
NM_001354689.1:c.989C>G
|
NP_001341618.1:p.Thr330Ser
|
|
|
NM_001354690.1:c.929C>G
|
NP_001341619.1:p.Thr310Ser
|
|
|
NM_001354691.1:c.686C>G
|
NP_001341620.1:p.Thr229Ser
|
|
|
NM_001354692.1:c.686C>G
|
NP_001341621.1:p.Thr229Ser
|
|
|
NM_001354693.1:c.830C>G
|
NP_001341622.1:p.Thr277Ser
|
|
|
NM_001354694.1:c.746C>G
|
NP_001341623.1:p.Thr249Ser
|
|
|
NM_001354695.1:c.587C>G
|
NP_001341624.1:p.Thr196Ser
|
|
|
NR_148940.1:n.1344C>G
|
|
|
|
NR_148941.1:n.1344C>G
|
|
|
|
NR_148942.1:n.1344C>G
|
|
|
|
XM_011533974.3:c.929C>G
|
XP_011532276.1:p.Thr310Ser
|
|
|
XM_017006966.1:c.830C>G
|
XP_016862455.1:p.Thr277Ser
|
|
|
XR_001740227.1:n.1161C>G
|
|
|
|
NM_001354689.3:c.989C>G
|
NP_001341618.1:p.Thr330Ser
|
|
|
NM_001354690.2:c.929C>G
|
NP_001341619.1:p.Thr310Ser
|
|
|
NM_001354691.2:c.686C>G
|
NP_001341620.1:p.Thr229Ser
|
|
|
NM_001354692.2:c.686C>G
|
NP_001341621.1:p.Thr229Ser
|
|
|
NM_001354693.2:c.830C>G
|
NP_001341622.1:p.Thr277Ser
|
|
|
NM_001354694.2:c.746C>G
|
NP_001341623.1:p.Thr249Ser
|
|
|
NM_001354695.2:c.587C>G
|
NP_001341624.1:p.Thr196Ser
|
|
|
NR_148940.2:n.1260C>G
|
|
|
|
NR_148941.2:n.1260C>G
|
|
|
|
NR_148942.2:n.1260C>G
|
|
|
|
NM_001354690.3:c.929C>G
|
NP_001341619.1:p.Thr310Ser
|
|
|
NM_001354691.3:c.686C>G
|
NP_001341620.1:p.Thr229Ser
|
|
|
NM_001354692.3:c.686C>G
|
NP_001341621.1:p.Thr229Ser
|
|
|
NM_001354693.3:c.830C>G
|
NP_001341622.1:p.Thr277Ser
|
|
|
NM_001354694.3:c.746C>G
|
NP_001341623.1:p.Thr249Ser
|
|
|
NM_001354695.3:c.587C>G
|
NP_001341624.1:p.Thr196Ser
|
|
|
NM_002880.4:c.929C>G
MANE Select
|
NP_002871.1:p.Thr310Ser
|
|
|
NR_148940.3:n.1260C>G
|
|
|
|
NR_148941.3:n.1260C>G
|
|
|
|
NR_148942.3:n.1260C>G
|
|
|
