ENST00000356592.8:c.1327A>G
|
|
|
ENST00000361925.9:c.1422A>G
|
ENSP00000354651.5:p.Ile474Met
|
|
ENST00000523372.2:c.1385A>G
|
|
|
ENST00000638253.1:n.580A>G
|
|
|
ENST00000638552.1:c.1017A>G
|
ENSP00000491763.1:p.Ile339Met
|
|
ENST00000638660.1:c.1041A>G
|
ENSP00000492869.1:p.Ile347Met
|
|
ENST00000638772.1:c.*3923A>G
|
ENSP00000491557.1:n.*3923A>G
|
|
ENST00000638877.1:c.1203A>G
|
|
|
ENST00000639046.1:c.693A>G
|
ENSP00000492659.1:p.Ile231Met
|
|
ENST00000639111.2:c.1302A>G
|
ENSP00000492125.2:p.Ile434Met
|
|
ENST00000639213.2:c.1326A>G
MANE Select
|
ENSP00000491909.2:p.Ile442Met
|
|
ENST00000639278.1:c.1989A>G
|
ENSP00000491958.1:n.1989A>G
|
|
ENST00000639384.1:c.*1507A>G
|
ENSP00000491240.1:n.*1507A>G
|
|
ENST00000639424.1:c.*526A>G
|
ENSP00000491245.1:n.*526A>G
|
|
ENST00000639683.1:c.1260A>G
|
ENSP00000492581.1:p.Ile420Met
|
|
ENST00000639975.1:c.1236A>G
|
ENSP00000492096.1:p.Ile412Met
|
|
ENST00000640500.1:n.600A>G
|
|
|
ENST00000640739.1:n.6273A>G
|
|
|
ENST00000640910.1:c.764A>G
|
|
|
ENST00000640985.1:c.1239A>G
|
ENSP00000492293.1:p.Ile413Met
|
|
ENST00000641017.1:c.1395A>G
|
ENSP00000493461.1:p.Ile465Met
|
|
ENST00000356592.7:c.1326A>G
|
ENSP00000349000.3:p.Ile442Met
|
|
ENST00000361925.8:c.1302A>G
|
ENSP00000354651.4:p.Ile434Met
|
|
ENST00000414552.6:c.1446A>G
|
ENSP00000410732.2:p.Ile482Met
|
|
ENST00000522990.5:c.*904A>G
|
ENSP00000430732.1:n.*904A>G
|
|
ENST00000523372.1:c.1423A>G
|
ENSP00000430124.1:n.1423A>G
|
|
NM_000816.3:c.1302A>G
|
NP_000807.2:p.Ile434Met
|
|
NM_198903.2:c.1446A>G
|
NP_944493.2:p.Ile482Met
|
|
NM_198904.2:c.1326A>G
|
NP_944494.1:p.Ile442Met
|
|
NM_001375339.1:c.1317A>G
|
NP_001362268.1:p.Ile439Met
|
|
NM_001375340.1:c.*160A>G
|
NP_001362269.1:n.*160A>G
|
|
NM_001375341.1:c.1323A>G
|
NP_001362270.1:p.Ile441Met
|
|
NM_001375342.1:c.1299A>G
|
NP_001362271.1:p.Ile433Met
|
|
NM_001375343.1:c.1422A>G
|
NP_001362272.1:p.Ile474Met
|
|
NM_001375344.1:c.1365A>G
|
NP_001362273.1:p.Ile455Met
|
|
NM_001375345.1:c.1236A>G
|
NP_001362274.1:p.Ile412Met
|
|
NM_001375346.1:c.1260A>G
|
NP_001362275.1:p.Ile420Met
|
|
NM_001375347.1:c.1239A>G
|
NP_001362276.1:p.Ile413Met
|
|
NM_001375348.1:c.882A>G
|
NP_001362277.1:p.Ile294Met
|
|
NM_001375349.1:c.1017A>G
|
NP_001362278.1:p.Ile339Met
|
|
NM_001375350.1:c.906A>G
|
NP_001362279.1:p.Ile302Met
|
|
NM_198904.3:c.1326A>G
|
NP_944494.1:p.Ile442Met
|
|
NM_198904.4:c.1326A>G
MANE Select
|
NP_944494.1:p.Ile442Met
|
|