ENST00000356592.8:c.1299G=
|
|
|
ENST00000361925.9:c.1394G=
|
ENSP00000354651.5:p.Arg465=
|
|
ENST00000523372.2:c.1357G=
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|
|
ENST00000638253.1:n.552G=
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|
|
ENST00000638552.1:c.989G=
|
ENSP00000491763.1:p.Arg330=
|
|
ENST00000638660.1:c.1013G=
|
ENSP00000492869.1:p.Arg338=
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|
ENST00000638772.1:c.*3895G=
|
ENSP00000491557.1:n.*3895G=
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|
ENST00000638877.1:c.1175G=
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|
|
ENST00000639046.1:c.665G=
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ENSP00000492659.1:p.Arg222=
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ENST00000639111.2:c.1274G=
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ENSP00000492125.2:p.Arg425=
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|
ENST00000639213.2:c.1298G=
MANE Select
|
ENSP00000491909.2:p.Arg433=
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|
ENST00000639278.1:c.1961G=
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ENSP00000491958.1:n.1961G=
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|
ENST00000639384.1:c.*1479G=
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ENSP00000491240.1:n.*1479G=
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ENST00000639424.1:c.*498G=
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ENSP00000491245.1:n.*498G=
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|
ENST00000639683.1:c.1232G=
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ENSP00000492581.1:p.Arg411=
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|
ENST00000639975.1:c.1208G=
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ENSP00000492096.1:p.Arg403=
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ENST00000640500.1:n.572G=
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ENST00000640739.1:n.6245G=
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ENST00000640910.1:c.736G=
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ENST00000640985.1:c.1211G=
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ENSP00000492293.1:p.Arg404=
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ENST00000641017.1:c.1367G=
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ENSP00000493461.1:p.Arg456=
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|
ENST00000356592.7:c.1298G=
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ENSP00000349000.3:p.Arg433=
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|
ENST00000361925.8:c.1274G=
|
ENSP00000354651.4:p.Arg425=
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|
ENST00000414552.6:c.1418G=
|
ENSP00000410732.2:p.Arg473=
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|
ENST00000522990.5:c.*876G=
|
ENSP00000430732.1:n.*876G=
|
|
ENST00000523372.1:c.1395G=
|
ENSP00000430124.1:n.1395G=
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|
NM_000816.3:c.1274G=
|
NP_000807.2:p.Arg425=
|
|
NM_198903.2:c.1418G=
|
NP_944493.2:p.Arg473=
|
|
NM_198904.2:c.1298G=
|
NP_944494.1:p.Arg433=
|
|
NM_001375339.1:c.1289G=
|
NP_001362268.1:p.Arg430=
|
|
NM_001375340.1:c.*132G=
|
NP_001362269.1:n.*132G=
|
|
NM_001375341.1:c.1295G=
|
NP_001362270.1:p.Arg432=
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|
NM_001375342.1:c.1271G=
|
NP_001362271.1:p.Arg424=
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|
NM_001375343.1:c.1394G=
|
NP_001362272.1:p.Arg465=
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|
NM_001375344.1:c.1337G=
|
NP_001362273.1:p.Arg446=
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|
NM_001375345.1:c.1208G=
|
NP_001362274.1:p.Arg403=
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|
NM_001375346.1:c.1232G=
|
NP_001362275.1:p.Arg411=
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|
NM_001375347.1:c.1211G=
|
NP_001362276.1:p.Arg404=
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|
NM_001375348.1:c.854G=
|
NP_001362277.1:p.Arg285=
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|
NM_001375349.1:c.989G=
|
NP_001362278.1:p.Arg330=
|
|
NM_001375350.1:c.878G=
|
NP_001362279.1:p.Arg293=
|
|
NM_198904.3:c.1298G=
|
NP_944494.1:p.Arg433=
|
|
NM_198904.4:c.1298G=
MANE Select
|
NP_944494.1:p.Arg433=
|
|