|
ENST00000423275.6:c.*643G>T
|
ENSP00000401088.1:n.*643G>T
|
|
|
ENST00000432427.3:c.298G>T
|
|
|
|
ENST00000465826.6:n.569G>T
|
|
|
|
ENST00000491290.2:n.1355G>T
|
|
|
|
ENST00000684903.1:c.*655G>T
|
ENSP00000508612.1:n.*655G>T
|
|
|
ENST00000685348.1:c.*655G>T
|
ENSP00000510285.1:n.*655G>T
|
|
|
ENST00000685437.1:c.879G>T
|
ENSP00000508794.1:p.Glu293Asp
|
|
|
ENST00000685653.1:c.978G>T
|
ENSP00000509968.1:p.Glu326Asp
|
|
|
ENST00000685738.1:c.978G>T
|
ENSP00000510156.1:p.Glu326Asp
|
|
|
ENST00000686409.1:n.1686G>T
|
|
|
|
ENST00000686455.1:n.1341G>T
|
|
|
|
ENST00000686479.1:n.1349G>T
|
|
|
|
ENST00000686762.1:c.978G>T
|
ENSP00000509767.1:p.Glu326Asp
|
|
|
ENST00000687257.1:n.1214G>T
|
|
|
|
ENST00000687326.1:c.978G>T
|
ENSP00000509665.1:p.Glu326Asp
|
|
|
ENST00000687486.1:c.182+224G>T
|
|
|
|
ENST00000687505.1:n.1096G>T
|
|
|
|
ENST00000687923.1:c.879G>T
|
ENSP00000510255.1:p.Glu293Asp
|
|
|
ENST00000687940.1:n.1355G>T
|
|
|
|
ENST00000688269.1:n.1574G>T
|
|
|
|
ENST00000688326.1:c.298G>T
|
|
|
|
ENST00000688444.1:n.1304G>T
|
|
|
|
ENST00000688543.1:c.879G>T
|
ENSP00000509612.1:p.Glu293Asp
|
|
|
ENST00000688625.1:c.*556G>T
|
ENSP00000509522.1:n.*556G>T
|
|
|
ENST00000688803.1:n.1209G>T
|
|
|
|
ENST00000689097.1:c.*655G>T
|
ENSP00000509756.1:n.*655G>T
|
|
|
ENST00000689389.1:c.978G>T
|
ENSP00000510213.1:p.Glu326Asp
|
|
|
ENST00000689418.1:c.*655G>T
|
ENSP00000509467.1:n.*655G>T
|
|
|
ENST00000689481.1:c.*655G>T
|
ENSP00000510248.1:n.*655G>T
|
|
|
ENST00000689540.1:n.1128G>T
|
|
|
|
ENST00000689876.1:c.978G>T
|
ENSP00000508535.1:p.Glu326Asp
|
|
|
ENST00000689914.1:c.978G>T
|
ENSP00000509847.1:p.Glu326Asp
|
|
|
ENST00000690397.1:c.867G>T
|
ENSP00000508730.1:p.Glu289Asp
|
|
|
ENST00000690460.1:c.966G>T
|
ENSP00000509106.1:p.Glu322Asp
|
|
|
ENST00000690625.1:n.1281G>T
|
|
|
|
ENST00000691268.1:c.405G>T
|
|
|
|
ENST00000691396.1:c.*771G>T
|
ENSP00000510712.1:n.*771G>T
|
|
|
ENST00000691724.1:c.978G>T
|
ENSP00000509255.1:p.Glu326Asp
|
|
|
ENST00000691779.1:c.*556G>T
|
ENSP00000508592.1:n.*556G>T
|
|
|
ENST00000691899.1:c.978G>T
|
ENSP00000508763.1:p.Glu326Asp
|
|
|
ENST00000692069.1:n.1201G>T
|
|
|
|
ENST00000692093.1:c.879G>T
|
ENSP00000509669.1:p.Glu293Asp
|
|
|
ENST00000692311.1:n.1459G>T
|
|
|
|
ENST00000692558.1:n.1343G>T
|
|
|
|
ENST00000692773.1:c.*715G>T
|
ENSP00000509055.1:n.*715G>T
|
|
|
ENST00000692830.1:c.*723G>T
|
ENSP00000509461.1:n.*723G>T
|
|
|
ENST00000693069.1:c.879G>T
|
ENSP00000510072.1:p.Glu293Asp
|
|
|
ENST00000693312.1:c.753G>T
|
ENSP00000508686.1:p.Glu251Asp
|
|
|
ENST00000693664.1:c.978G>T
|
ENSP00000509614.1:p.Glu326Asp
|
|
|
ENST00000693705.1:c.*655G>T
|
ENSP00000510697.1:n.*655G>T
|
|
|
ENST00000251849.9:c.978G>T
MANE Select
|
ENSP00000251849.4:p.Glu326Asp
|
|
|
ENST00000442415.7:c.1038G>T
|
ENSP00000401888.2:p.Glu346Asp
|
|
|
ENST00000251849.8:c.978G>T
|
ENSP00000251849.4:p.Glu326Asp
|
|
|
ENST00000423275.5:c.*655G>T
|
ENSP00000401088.1:n.*655G>T
|
|
|
ENST00000432427.2:c.615G>T
|
ENSP00000398591.2:p.Glu205Asp
|
|
|
ENST00000442415.6:c.1038G>T
|
ENSP00000401888.2:p.Glu346Asp
|
|
|
ENST00000465826.5:n.222G>T
|
|
|
|
NM_002880.3:c.978G>T , LRG_413t1:c.978G>T
|
NP_002871.1:p.Glu326Asp
|
|
|
XM_005265355.1:c.978G>T
|
XP_005265412.1:p.Glu326Asp
|
|
|
XM_005265357.1:c.879G>T
|
XP_005265414.1:p.Glu293Asp
|
|
|
XM_005265358.3:c.735G>T
|
XP_005265415.1:p.Glu245Asp
|
|
|
XM_005265359.3:c.636G>T
|
XP_005265416.1:p.Glu212Asp
|
|
|
XM_005265360.1:c.978G>T
|
XP_005265417.1:p.Glu326Asp
|
|
|
XM_011533974.1:c.978G>T
|
XP_011532276.1:p.Glu326Asp
|
|
|
XM_011533975.1:c.735G>T
|
XP_011532277.1:p.Glu245Asp
|
|
|
NM_001354689.1:c.1038G>T
|
NP_001341618.1:p.Glu346Asp
|
|
|
NM_001354690.1:c.978G>T
|
NP_001341619.1:p.Glu326Asp
|
|
|
NM_001354691.1:c.735G>T
|
NP_001341620.1:p.Glu245Asp
|
|
|
NM_001354692.1:c.735G>T
|
NP_001341621.1:p.Glu245Asp
|
|
|
NM_001354693.1:c.879G>T
|
NP_001341622.1:p.Glu293Asp
|
|
|
NM_001354694.1:c.795G>T
|
NP_001341623.1:p.Glu265Asp
|
|
|
NM_001354695.1:c.636G>T
|
NP_001341624.1:p.Glu212Asp
|
|
|
NR_148940.1:n.1393G>T
|
|
|
|
NR_148941.1:n.1393G>T
|
|
|
|
NR_148942.1:n.1393G>T
|
|
|
|
XM_011533974.3:c.978G>T
|
XP_011532276.1:p.Glu326Asp
|
|
|
XM_017006966.1:c.879G>T
|
XP_016862455.1:p.Glu293Asp
|
|
|
XR_001740227.1:n.1210G>T
|
|
|
|
NM_001354689.3:c.1038G>T
|
NP_001341618.1:p.Glu346Asp
|
|
|
NM_001354690.2:c.978G>T
|
NP_001341619.1:p.Glu326Asp
|
|
|
NM_001354691.2:c.735G>T
|
NP_001341620.1:p.Glu245Asp
|
|
|
NM_001354692.2:c.735G>T
|
NP_001341621.1:p.Glu245Asp
|
|
|
NM_001354693.2:c.879G>T
|
NP_001341622.1:p.Glu293Asp
|
|
|
NM_001354694.2:c.795G>T
|
NP_001341623.1:p.Glu265Asp
|
|
|
NM_001354695.2:c.636G>T
|
NP_001341624.1:p.Glu212Asp
|
|
|
NR_148940.2:n.1309G>T
|
|
|
|
NR_148941.2:n.1309G>T
|
|
|
|
NR_148942.2:n.1309G>T
|
|
|
|
NM_001354690.3:c.978G>T
|
NP_001341619.1:p.Glu326Asp
|
|
|
NM_001354691.3:c.735G>T
|
NP_001341620.1:p.Glu245Asp
|
|
|
NM_001354692.3:c.735G>T
|
NP_001341621.1:p.Glu245Asp
|
|
|
NM_001354693.3:c.879G>T
|
NP_001341622.1:p.Glu293Asp
|
|
|
NM_001354694.3:c.795G>T
|
NP_001341623.1:p.Glu265Asp
|
|
|
NM_001354695.3:c.636G>T
|
NP_001341624.1:p.Glu212Asp
|
|
|
NM_002880.4:c.978G>T
MANE Select
|
NP_002871.1:p.Glu326Asp
|
|
|
NR_148940.3:n.1309G>T
|
|
|
|
NR_148941.3:n.1309G>T
|
|
|
|
NR_148942.3:n.1309G>T
|
|
|
