|
ENST00000423275.6:c.*552G>C
|
ENSP00000401088.1:n.*552G>C
|
|
|
ENST00000432427.3:c.207G>C
|
|
|
|
ENST00000465826.6:n.478G>C
|
|
|
|
ENST00000491290.2:n.1264G>C
|
|
|
|
ENST00000684903.1:c.*564G>C
|
ENSP00000508612.1:n.*564G>C
|
|
|
ENST00000685348.1:c.*564G>C
|
ENSP00000510285.1:n.*564G>C
|
|
|
ENST00000685437.1:c.788G>C
|
ENSP00000508794.1:p.Ser263Thr
|
|
|
ENST00000685438.1:n.651G>C
|
|
|
|
ENST00000685653.1:c.887G>C
|
ENSP00000509968.1:p.Ser296Thr
|
|
|
ENST00000685738.1:c.887G>C
|
ENSP00000510156.1:p.Ser296Thr
|
|
|
ENST00000686409.1:n.1595G>C
|
|
|
|
ENST00000686455.1:n.1250G>C
|
|
|
|
ENST00000686479.1:n.1258G>C
|
|
|
|
ENST00000686762.1:c.887G>C
|
ENSP00000509767.1:p.Ser296Thr
|
|
|
ENST00000687257.1:n.1123G>C
|
|
|
|
ENST00000687326.1:c.887G>C
|
ENSP00000509665.1:p.Ser296Thr
|
|
|
ENST00000687486.1:c.182+133G>C
|
|
|
|
ENST00000687505.1:n.1005G>C
|
|
|
|
ENST00000687923.1:c.788G>C
|
ENSP00000510255.1:p.Ser263Thr
|
|
|
ENST00000687940.1:n.1264G>C
|
|
|
|
ENST00000688269.1:n.1483G>C
|
|
|
|
ENST00000688326.1:c.207G>C
|
|
|
|
ENST00000688444.1:n.1213G>C
|
|
|
|
ENST00000688543.1:c.788G>C
|
ENSP00000509612.1:p.Ser263Thr
|
|
|
ENST00000688625.1:c.*465G>C
|
ENSP00000509522.1:n.*465G>C
|
|
|
ENST00000688803.1:n.1118G>C
|
|
|
|
ENST00000689097.1:c.*564G>C
|
ENSP00000509756.1:n.*564G>C
|
|
|
ENST00000689389.1:c.887G>C
|
ENSP00000510213.1:p.Ser296Thr
|
|
|
ENST00000689418.1:c.*564G>C
|
ENSP00000509467.1:n.*564G>C
|
|
|
ENST00000689481.1:c.*564G>C
|
ENSP00000510248.1:n.*564G>C
|
|
|
ENST00000689540.1:n.1037G>C
|
|
|
|
ENST00000689876.1:c.887G>C
|
ENSP00000508535.1:p.Ser296Thr
|
|
|
ENST00000689914.1:c.887G>C
|
ENSP00000509847.1:p.Ser296Thr
|
|
|
ENST00000690397.1:c.776G>C
|
ENSP00000508730.1:p.Ser259Thr
|
|
|
ENST00000690460.1:c.875G>C
|
ENSP00000509106.1:p.Ser292Thr
|
|
|
ENST00000690625.1:n.1190G>C
|
|
|
|
ENST00000691268.1:c.314G>C
|
|
|
|
ENST00000691396.1:c.*680G>C
|
ENSP00000510712.1:n.*680G>C
|
|
|
ENST00000691724.1:c.887G>C
|
ENSP00000509255.1:p.Ser296Thr
|
|
|
ENST00000691779.1:c.*465G>C
|
ENSP00000508592.1:n.*465G>C
|
|
|
ENST00000691899.1:c.887G>C
|
ENSP00000508763.1:p.Ser296Thr
|
|
|
ENST00000692069.1:n.1110G>C
|
|
|
|
ENST00000692093.1:c.788G>C
|
ENSP00000509669.1:p.Ser263Thr
|
|
|
ENST00000692311.1:n.1368G>C
|
|
|
|
ENST00000692558.1:n.1252G>C
|
|
|
|
ENST00000692773.1:c.*624G>C
|
ENSP00000509055.1:n.*624G>C
|
|
|
ENST00000692830.1:c.*632G>C
|
ENSP00000509461.1:n.*632G>C
|
|
|
ENST00000693069.1:c.788G>C
|
ENSP00000510072.1:p.Ser263Thr
|
|
|
ENST00000693312.1:c.662G>C
|
ENSP00000508686.1:p.Ser221Thr
|
|
|
ENST00000693664.1:c.887G>C
|
ENSP00000509614.1:p.Ser296Thr
|
|
|
ENST00000693705.1:c.*564G>C
|
ENSP00000510697.1:n.*564G>C
|
|
|
ENST00000251849.9:c.887G>C
MANE Select
|
ENSP00000251849.4:p.Ser296Thr
|
|
|
ENST00000442415.7:c.947G>C
|
ENSP00000401888.2:p.Ser316Thr
|
|
|
ENST00000251849.8:c.887G>C
|
ENSP00000251849.4:p.Ser296Thr
|
|
|
ENST00000423275.5:c.*564G>C
|
ENSP00000401088.1:n.*564G>C
|
|
|
ENST00000432427.2:c.524G>C
|
ENSP00000398591.2:p.Ser175Thr
|
|
|
ENST00000442415.6:c.947G>C
|
ENSP00000401888.2:p.Ser316Thr
|
|
|
ENST00000465826.5:n.131G>C
|
|
|
|
ENST00000491290.1:n.516G>C
|
|
|
|
NM_002880.3:c.887G>C , LRG_413t1:c.887G>C
|
NP_002871.1:p.Ser296Thr
|
|
|
XM_005265355.1:c.887G>C
|
XP_005265412.1:p.Ser296Thr
|
|
|
XM_005265357.1:c.788G>C
|
XP_005265414.1:p.Ser263Thr
|
|
|
XM_005265358.3:c.644G>C
|
XP_005265415.1:p.Ser215Thr
|
|
|
XM_005265359.3:c.545G>C
|
XP_005265416.1:p.Ser182Thr
|
|
|
XM_005265360.1:c.887G>C
|
XP_005265417.1:p.Ser296Thr
|
|
|
XM_011533974.1:c.887G>C
|
XP_011532276.1:p.Ser296Thr
|
|
|
XM_011533975.1:c.644G>C
|
XP_011532277.1:p.Ser215Thr
|
|
|
NM_001354689.1:c.947G>C
|
NP_001341618.1:p.Ser316Thr
|
|
|
NM_001354690.1:c.887G>C
|
NP_001341619.1:p.Ser296Thr
|
|
|
NM_001354691.1:c.644G>C
|
NP_001341620.1:p.Ser215Thr
|
|
|
NM_001354692.1:c.644G>C
|
NP_001341621.1:p.Ser215Thr
|
|
|
NM_001354693.1:c.788G>C
|
NP_001341622.1:p.Ser263Thr
|
|
|
NM_001354694.1:c.704G>C
|
NP_001341623.1:p.Ser235Thr
|
|
|
NM_001354695.1:c.545G>C
|
NP_001341624.1:p.Ser182Thr
|
|
|
NR_148940.1:n.1302G>C
|
|
|
|
NR_148941.1:n.1302G>C
|
|
|
|
NR_148942.1:n.1302G>C
|
|
|
|
XM_011533974.3:c.887G>C
|
XP_011532276.1:p.Ser296Thr
|
|
|
XM_017006966.1:c.788G>C
|
XP_016862455.1:p.Ser263Thr
|
|
|
XR_001740227.1:n.1119G>C
|
|
|
|
NM_001354689.3:c.947G>C
|
NP_001341618.1:p.Ser316Thr
|
|
|
NM_001354690.2:c.887G>C
|
NP_001341619.1:p.Ser296Thr
|
|
|
NM_001354691.2:c.644G>C
|
NP_001341620.1:p.Ser215Thr
|
|
|
NM_001354692.2:c.644G>C
|
NP_001341621.1:p.Ser215Thr
|
|
|
NM_001354693.2:c.788G>C
|
NP_001341622.1:p.Ser263Thr
|
|
|
NM_001354694.2:c.704G>C
|
NP_001341623.1:p.Ser235Thr
|
|
|
NM_001354695.2:c.545G>C
|
NP_001341624.1:p.Ser182Thr
|
|
|
NR_148940.2:n.1218G>C
|
|
|
|
NR_148941.2:n.1218G>C
|
|
|
|
NR_148942.2:n.1218G>C
|
|
|
|
NM_001354690.3:c.887G>C
|
NP_001341619.1:p.Ser296Thr
|
|
|
NM_001354691.3:c.644G>C
|
NP_001341620.1:p.Ser215Thr
|
|
|
NM_001354692.3:c.644G>C
|
NP_001341621.1:p.Ser215Thr
|
|
|
NM_001354693.3:c.788G>C
|
NP_001341622.1:p.Ser263Thr
|
|
|
NM_001354694.3:c.704G>C
|
NP_001341623.1:p.Ser235Thr
|
|
|
NM_001354695.3:c.545G>C
|
NP_001341624.1:p.Ser182Thr
|
|
|
NM_002880.4:c.887G>C
MANE Select
|
NP_002871.1:p.Ser296Thr
|
|
|
NR_148940.3:n.1218G>C
|
|
|
|
NR_148941.3:n.1218G>C
|
|
|
|
NR_148942.3:n.1218G>C
|
|
|
