ENST00000356592.8:c.1331A>T
|
|
|
ENST00000361925.9:c.1426A>T
|
ENSP00000354651.5:p.Ile476Phe
|
|
ENST00000523372.2:c.1389A>T
|
|
|
ENST00000638253.1:n.584A>T
|
|
|
ENST00000638552.1:c.1021A>T
|
ENSP00000491763.1:p.Ile341Phe
|
|
ENST00000638660.1:c.1045A>T
|
ENSP00000492869.1:p.Ile349Phe
|
|
ENST00000638772.1:c.*3927A>T
|
ENSP00000491557.1:n.*3927A>T
|
|
ENST00000638877.1:c.1207A>T
|
|
|
ENST00000639046.1:c.697A>T
|
ENSP00000492659.1:p.Ile233Phe
|
|
ENST00000639111.2:c.1306A>T
|
ENSP00000492125.2:p.Ile436Phe
|
|
ENST00000639213.2:c.1330A>T
MANE Select
|
ENSP00000491909.2:p.Ile444Phe
|
|
ENST00000639278.1:c.1993A>T
|
ENSP00000491958.1:n.1993A>T
|
|
ENST00000639384.1:c.*1511A>T
|
ENSP00000491240.1:n.*1511A>T
|
|
ENST00000639424.1:c.*530A>T
|
ENSP00000491245.1:n.*530A>T
|
|
ENST00000639683.1:c.1264A>T
|
ENSP00000492581.1:p.Ile422Phe
|
|
ENST00000639975.1:c.1240A>T
|
ENSP00000492096.1:p.Ile414Phe
|
|
ENST00000640500.1:n.604A>T
|
|
|
ENST00000640739.1:n.6277A>T
|
|
|
ENST00000640910.1:c.768A>T
|
|
|
ENST00000640985.1:c.1243A>T
|
ENSP00000492293.1:p.Ile415Phe
|
|
ENST00000641017.1:c.1399A>T
|
ENSP00000493461.1:p.Ile467Phe
|
|
ENST00000356592.7:c.1330A>T
|
ENSP00000349000.3:p.Ile444Phe
|
|
ENST00000361925.8:c.1306A>T
|
ENSP00000354651.4:p.Ile436Phe
|
|
ENST00000414552.6:c.1450A>T
|
ENSP00000410732.2:p.Ile484Phe
|
|
ENST00000522990.5:c.*908A>T
|
ENSP00000430732.1:n.*908A>T
|
|
ENST00000523372.1:c.1427A>T
|
ENSP00000430124.1:n.1427A>T
|
|
NM_000816.3:c.1306A>T
|
NP_000807.2:p.Ile436Phe
|
|
NM_198903.2:c.1450A>T
|
NP_944493.2:p.Ile484Phe
|
|
NM_198904.2:c.1330A>T
|
NP_944494.1:p.Ile444Phe
|
|
NM_001375339.1:c.1321A>T
|
NP_001362268.1:p.Ile441Phe
|
|
NM_001375340.1:c.*164A>T
|
NP_001362269.1:n.*164A>T
|
|
NM_001375341.1:c.1327A>T
|
NP_001362270.1:p.Ile443Phe
|
|
NM_001375342.1:c.1303A>T
|
NP_001362271.1:p.Ile435Phe
|
|
NM_001375343.1:c.1426A>T
|
NP_001362272.1:p.Ile476Phe
|
|
NM_001375344.1:c.1369A>T
|
NP_001362273.1:p.Ile457Phe
|
|
NM_001375345.1:c.1240A>T
|
NP_001362274.1:p.Ile414Phe
|
|
NM_001375346.1:c.1264A>T
|
NP_001362275.1:p.Ile422Phe
|
|
NM_001375347.1:c.1243A>T
|
NP_001362276.1:p.Ile415Phe
|
|
NM_001375348.1:c.886A>T
|
NP_001362277.1:p.Ile296Phe
|
|
NM_001375349.1:c.1021A>T
|
NP_001362278.1:p.Ile341Phe
|
|
NM_001375350.1:c.910A>T
|
NP_001362279.1:p.Ile304Phe
|
|
NM_198904.3:c.1330A>T
|
NP_944494.1:p.Ile444Phe
|
|
NM_198904.4:c.1330A>T
MANE Select
|
NP_944494.1:p.Ile444Phe
|
|