ENST00000356592.8:c.1280T=
|
|
|
ENST00000361925.9:c.1375T=
|
ENSP00000354651.5:p.Cys459=
|
|
ENST00000523372.2:c.1338T=
|
|
|
ENST00000638253.1:n.533T=
|
|
|
ENST00000638552.1:c.970T=
|
ENSP00000491763.1:p.Cys324=
|
|
ENST00000638660.1:c.994T=
|
ENSP00000492869.1:p.Cys332=
|
|
ENST00000638772.1:c.*3876T=
|
ENSP00000491557.1:n.*3876T=
|
|
ENST00000638877.1:c.1156T=
|
|
|
ENST00000639046.1:c.646T=
|
ENSP00000492659.1:p.Cys216=
|
|
ENST00000639111.2:c.1255T=
|
ENSP00000492125.2:p.Cys419=
|
|
ENST00000639213.2:c.1279T=
MANE Select
|
ENSP00000491909.2:p.Cys427=
|
|
ENST00000639278.1:c.1942T=
|
ENSP00000491958.1:n.1942T=
|
|
ENST00000639384.1:c.*1460T=
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ENSP00000491240.1:n.*1460T=
|
|
ENST00000639424.1:c.*479T=
|
ENSP00000491245.1:n.*479T=
|
|
ENST00000639683.1:c.1213T=
|
ENSP00000492581.1:p.Cys405=
|
|
ENST00000639975.1:c.1189T=
|
ENSP00000492096.1:p.Cys397=
|
|
ENST00000640500.1:n.553T=
|
|
|
ENST00000640739.1:n.6226T=
|
|
|
ENST00000640910.1:c.717T=
|
|
|
ENST00000640985.1:c.1192T=
|
ENSP00000492293.1:p.Cys398=
|
|
ENST00000641017.1:c.1348T=
|
ENSP00000493461.1:p.Cys450=
|
|
ENST00000356592.7:c.1279T=
|
ENSP00000349000.3:p.Cys427=
|
|
ENST00000361925.8:c.1255T=
|
ENSP00000354651.4:p.Cys419=
|
|
ENST00000414552.6:c.1399T=
|
ENSP00000410732.2:p.Cys467=
|
|
ENST00000522990.5:c.*857T=
|
ENSP00000430732.1:n.*857T=
|
|
ENST00000523372.1:c.1376T=
|
ENSP00000430124.1:n.1376T=
|
|
NM_000816.3:c.1255T=
|
NP_000807.2:p.Cys419=
|
|
NM_198903.2:c.1399T=
|
NP_944493.2:p.Cys467=
|
|
NM_198904.2:c.1279T=
|
NP_944494.1:p.Cys427=
|
|
NM_001375339.1:c.1270T=
|
NP_001362268.1:p.Cys424=
|
|
NM_001375340.1:c.*113T=
|
NP_001362269.1:n.*113T=
|
|
NM_001375341.1:c.1276T=
|
NP_001362270.1:p.Cys426=
|
|
NM_001375342.1:c.1252T=
|
NP_001362271.1:p.Cys418=
|
|
NM_001375343.1:c.1375T=
|
NP_001362272.1:p.Cys459=
|
|
NM_001375344.1:c.1318T=
|
NP_001362273.1:p.Cys440=
|
|
NM_001375345.1:c.1189T=
|
NP_001362274.1:p.Cys397=
|
|
NM_001375346.1:c.1213T=
|
NP_001362275.1:p.Cys405=
|
|
NM_001375347.1:c.1192T=
|
NP_001362276.1:p.Cys398=
|
|
NM_001375348.1:c.835T=
|
NP_001362277.1:p.Cys279=
|
|
NM_001375349.1:c.970T=
|
NP_001362278.1:p.Cys324=
|
|
NM_001375350.1:c.859T=
|
NP_001362279.1:p.Cys287=
|
|
NM_198904.3:c.1279T=
|
NP_944494.1:p.Cys427=
|
|
NM_198904.4:c.1279T=
MANE Select
|
NP_944494.1:p.Cys427=
|
|