ENST00000356592.8:c.1332T>C
|
|
|
ENST00000361925.9:c.1427T>C
|
ENSP00000354651.5:p.Ile476Thr
|
|
ENST00000523372.2:c.1390T>C
|
|
|
ENST00000638253.1:n.585T>C
|
|
|
ENST00000638552.1:c.1022T>C
|
ENSP00000491763.1:p.Ile341Thr
|
|
ENST00000638660.1:c.1046T>C
|
ENSP00000492869.1:p.Ile349Thr
|
|
ENST00000638772.1:c.*3928T>C
|
ENSP00000491557.1:n.*3928T>C
|
|
ENST00000638877.1:c.1208T>C
|
|
|
ENST00000639046.1:c.698T>C
|
ENSP00000492659.1:p.Ile233Thr
|
|
ENST00000639111.2:c.1307T>C
|
ENSP00000492125.2:p.Ile436Thr
|
|
ENST00000639213.2:c.1331T>C
MANE Select
|
ENSP00000491909.2:p.Ile444Thr
|
|
ENST00000639278.1:c.1994T>C
|
ENSP00000491958.1:n.1994T>C
|
|
ENST00000639384.1:c.*1512T>C
|
ENSP00000491240.1:n.*1512T>C
|
|
ENST00000639424.1:c.*531T>C
|
ENSP00000491245.1:n.*531T>C
|
|
ENST00000639683.1:c.1265T>C
|
ENSP00000492581.1:p.Ile422Thr
|
|
ENST00000639975.1:c.1241T>C
|
ENSP00000492096.1:p.Ile414Thr
|
|
ENST00000640500.1:n.605T>C
|
|
|
ENST00000640739.1:n.6278T>C
|
|
|
ENST00000640910.1:c.769T>C
|
|
|
ENST00000640985.1:c.1244T>C
|
ENSP00000492293.1:p.Ile415Thr
|
|
ENST00000641017.1:c.1400T>C
|
ENSP00000493461.1:p.Ile467Thr
|
|
ENST00000356592.7:c.1331T>C
|
ENSP00000349000.3:p.Ile444Thr
|
|
ENST00000361925.8:c.1307T>C
|
ENSP00000354651.4:p.Ile436Thr
|
|
ENST00000414552.6:c.1451T>C
|
ENSP00000410732.2:p.Ile484Thr
|
|
ENST00000522990.5:c.*909T>C
|
ENSP00000430732.1:n.*909T>C
|
|
ENST00000523372.1:c.1428T>C
|
ENSP00000430124.1:n.1428T>C
|
|
NM_000816.3:c.1307T>C
|
NP_000807.2:p.Ile436Thr
|
|
NM_198903.2:c.1451T>C
|
NP_944493.2:p.Ile484Thr
|
|
NM_198904.2:c.1331T>C
|
NP_944494.1:p.Ile444Thr
|
|
NM_001375339.1:c.1322T>C
|
NP_001362268.1:p.Ile441Thr
|
|
NM_001375340.1:c.*165T>C
|
NP_001362269.1:n.*165T>C
|
|
NM_001375341.1:c.1328T>C
|
NP_001362270.1:p.Ile443Thr
|
|
NM_001375342.1:c.1304T>C
|
NP_001362271.1:p.Ile435Thr
|
|
NM_001375343.1:c.1427T>C
|
NP_001362272.1:p.Ile476Thr
|
|
NM_001375344.1:c.1370T>C
|
NP_001362273.1:p.Ile457Thr
|
|
NM_001375345.1:c.1241T>C
|
NP_001362274.1:p.Ile414Thr
|
|
NM_001375346.1:c.1265T>C
|
NP_001362275.1:p.Ile422Thr
|
|
NM_001375347.1:c.1244T>C
|
NP_001362276.1:p.Ile415Thr
|
|
NM_001375348.1:c.887T>C
|
NP_001362277.1:p.Ile296Thr
|
|
NM_001375349.1:c.1022T>C
|
NP_001362278.1:p.Ile341Thr
|
|
NM_001375350.1:c.911T>C
|
NP_001362279.1:p.Ile304Thr
|
|
NM_198904.3:c.1331T>C
|
NP_944494.1:p.Ile444Thr
|
|
NM_198904.4:c.1331T>C
MANE Select
|
NP_944494.1:p.Ile444Thr
|
|