ENST00000356592.8:c.1383T>C
|
|
|
ENST00000361925.9:c.1478T>C
|
ENSP00000354651.5:p.Phe493Ser
|
|
ENST00000523372.2:c.1441T>C
|
|
|
ENST00000638253.1:n.636T>C
|
|
|
ENST00000638552.1:c.1073T>C
|
ENSP00000491763.1:p.Phe358Ser
|
|
ENST00000638660.1:c.1097T>C
|
ENSP00000492869.1:p.Phe366Ser
|
|
ENST00000638772.1:c.*3979T>C
|
ENSP00000491557.1:n.*3979T>C
|
|
ENST00000638877.1:c.1259T>C
|
|
|
ENST00000639046.1:c.749T>C
|
ENSP00000492659.1:p.Phe250Ser
|
|
ENST00000639111.2:c.1358T>C
|
ENSP00000492125.2:p.Phe453Ser
|
|
ENST00000639213.2:c.1382T>C
MANE Select
|
ENSP00000491909.2:p.Phe461Ser
|
|
ENST00000639278.1:c.2045T>C
|
ENSP00000491958.1:n.2045T>C
|
|
ENST00000639384.1:c.*1563T>C
|
ENSP00000491240.1:n.*1563T>C
|
|
ENST00000639424.1:c.*582T>C
|
ENSP00000491245.1:n.*582T>C
|
|
ENST00000639683.1:c.1316T>C
|
ENSP00000492581.1:p.Phe439Ser
|
|
ENST00000639975.1:c.1292T>C
|
ENSP00000492096.1:p.Phe431Ser
|
|
ENST00000640500.1:n.656T>C
|
|
|
ENST00000640739.1:n.6329T>C
|
|
|
ENST00000640910.1:c.820T>C
|
|
|
ENST00000640985.1:c.1295T>C
|
ENSP00000492293.1:p.Phe432Ser
|
|
ENST00000641017.1:c.1451T>C
|
ENSP00000493461.1:p.Phe484Ser
|
|
ENST00000356592.7:c.1382T>C
|
ENSP00000349000.3:p.Phe461Ser
|
|
ENST00000361925.8:c.1358T>C
|
ENSP00000354651.4:p.Phe453Ser
|
|
ENST00000414552.6:c.1502T>C
|
ENSP00000410732.2:p.Phe501Ser
|
|
ENST00000522990.5:c.*960T>C
|
ENSP00000430732.1:n.*960T>C
|
|
ENST00000523372.1:c.1479T>C
|
ENSP00000430124.1:n.1479T>C
|
|
NM_000816.3:c.1358T>C
|
NP_000807.2:p.Phe453Ser
|
|
NM_198903.2:c.1502T>C
|
NP_944493.2:p.Phe501Ser
|
|
NM_198904.2:c.1382T>C
|
NP_944494.1:p.Phe461Ser
|
|
NM_001375339.1:c.1373T>C
|
NP_001362268.1:p.Phe458Ser
|
|
NM_001375340.1:c.*216T>C
|
NP_001362269.1:n.*216T>C
|
|
NM_001375341.1:c.1379T>C
|
NP_001362270.1:p.Phe460Ser
|
|
NM_001375342.1:c.1355T>C
|
NP_001362271.1:p.Phe452Ser
|
|
NM_001375343.1:c.1478T>C
|
NP_001362272.1:p.Phe493Ser
|
|
NM_001375344.1:c.1421T>C
|
NP_001362273.1:p.Phe474Ser
|
|
NM_001375345.1:c.1292T>C
|
NP_001362274.1:p.Phe431Ser
|
|
NM_001375346.1:c.1316T>C
|
NP_001362275.1:p.Phe439Ser
|
|
NM_001375347.1:c.1295T>C
|
NP_001362276.1:p.Phe432Ser
|
|
NM_001375348.1:c.938T>C
|
NP_001362277.1:p.Phe313Ser
|
|
NM_001375349.1:c.1073T>C
|
NP_001362278.1:p.Phe358Ser
|
|
NM_001375350.1:c.962T>C
|
NP_001362279.1:p.Phe321Ser
|
|
NM_198904.3:c.1382T>C
|
NP_944494.1:p.Phe461Ser
|
|
NM_198904.4:c.1382T>C
MANE Select
|
NP_944494.1:p.Phe461Ser
|
|