ENST00000356592.8:c.1072T>C
|
|
|
ENST00000361925.9:c.1191T>C
|
ENSP00000354651.5:p.His397=
|
|
ENST00000523372.2:c.1154T>C
|
|
|
ENST00000638253.1:n.325T>C
|
|
|
ENST00000638552.1:c.786T>C
|
ENSP00000491763.1:p.His262=
|
|
ENST00000638660.1:c.786T>C
|
ENSP00000492869.1:p.His262=
|
|
ENST00000638772.1:c.1071T>C
|
ENSP00000491557.1:p.His357=
|
|
ENST00000638877.1:c.948T>C
|
|
|
ENST00000639046.1:c.462T>C
|
ENSP00000492659.1:p.His154=
|
|
ENST00000639111.2:c.1071T>C
|
ENSP00000492125.2:p.His357=
|
|
ENST00000639213.2:c.1071T>C
MANE Select
|
ENSP00000491909.2:p.His357=
|
|
ENST00000639278.1:c.999T>C
|
ENSP00000491958.1:p.His333=
|
|
ENST00000639384.1:c.1071T>C
|
ENSP00000491240.1:p.His357=
|
|
ENST00000639424.1:c.*271T>C
|
ENSP00000491245.1:n.*271T>C
|
|
ENST00000639683.1:c.1005T>C
|
ENSP00000492581.1:p.His335=
|
|
ENST00000639975.1:c.1005T>C
|
ENSP00000492096.1:p.His335=
|
|
ENST00000640500.1:n.369T>C
|
|
|
ENST00000640574.1:c.786T>C
|
ENSP00000491582.1:p.His262=
|
|
ENST00000640739.1:n.3602T>C
|
|
|
ENST00000640910.1:c.509T>C
|
|
|
ENST00000640985.1:c.984T>C
|
ENSP00000492293.1:p.His328=
|
|
ENST00000641017.1:c.1071T>C
|
ENSP00000493461.1:p.His357=
|
|
ENST00000356592.7:c.1071T>C
|
ENSP00000349000.3:p.His357=
|
|
ENST00000361925.8:c.1071T>C
|
ENSP00000354651.4:p.His357=
|
|
ENST00000414552.6:c.1191T>C
|
ENSP00000410732.2:p.His397=
|
|
ENST00000522990.5:c.*673T>C
|
ENSP00000430732.1:n.*673T>C
|
|
ENST00000523372.1:c.1192T>C
|
ENSP00000430124.1:n.1192T>C
|
|
NM_000816.3:c.1071T>C
|
NP_000807.2:p.His357=
|
|
NM_198903.2:c.1191T>C
|
NP_944493.2:p.His397=
|
|
NM_198904.2:c.1071T>C
|
NP_944494.1:p.His357=
|
|
NM_001375339.1:c.1062T>C
|
NP_001362268.1:p.His354=
|
|
NM_001375340.1:c.923-2474T>C
|
NP_001362269.1:n.923-2474T>C
|
|
NM_001375341.1:c.1068T>C
|
NP_001362270.1:p.His356=
|
|
NM_001375342.1:c.1068T>C
|
NP_001362271.1:p.His356=
|
|
NM_001375343.1:c.1191T>C
|
NP_001362272.1:p.His397=
|
|
NM_001375344.1:c.1110T>C
|
NP_001362273.1:p.His370=
|
|
NM_001375345.1:c.1005T>C
|
NP_001362274.1:p.His335=
|
|
NM_001375346.1:c.1005T>C
|
NP_001362275.1:p.His335=
|
|
NM_001375347.1:c.984T>C
|
NP_001362276.1:p.His328=
|
|
NM_001375348.1:c.651T>C
|
NP_001362277.1:p.His217=
|
|
NM_001375349.1:c.786T>C
|
NP_001362278.1:p.His262=
|
|
NM_001375350.1:c.651T>C
|
NP_001362279.1:p.His217=
|
|
NM_198904.3:c.1071T>C
|
NP_944494.1:p.His357=
|
|
NM_198904.4:c.1071T>C
MANE Select
|
NP_944494.1:p.His357=
|
|