ENST00000356592.8:c.1339T>A
|
|
|
ENST00000361925.9:c.1434T>A
|
ENSP00000354651.5:p.Ile478=
|
|
ENST00000523372.2:c.1397T>A
|
|
|
ENST00000638253.1:n.592T>A
|
|
|
ENST00000638552.1:c.1029T>A
|
ENSP00000491763.1:p.Ile343=
|
|
ENST00000638660.1:c.1053T>A
|
ENSP00000492869.1:p.Ile351=
|
|
ENST00000638772.1:c.*3935T>A
|
ENSP00000491557.1:n.*3935T>A
|
|
ENST00000638877.1:c.1215T>A
|
|
|
ENST00000639046.1:c.705T>A
|
ENSP00000492659.1:p.Ile235=
|
|
ENST00000639111.2:c.1314T>A
|
ENSP00000492125.2:p.Ile438=
|
|
ENST00000639213.2:c.1338T>A
MANE Select
|
ENSP00000491909.2:p.Ile446=
|
|
ENST00000639278.1:c.2001T>A
|
ENSP00000491958.1:n.2001T>A
|
|
ENST00000639384.1:c.*1519T>A
|
ENSP00000491240.1:n.*1519T>A
|
|
ENST00000639424.1:c.*538T>A
|
ENSP00000491245.1:n.*538T>A
|
|
ENST00000639683.1:c.1272T>A
|
ENSP00000492581.1:p.Ile424=
|
|
ENST00000639975.1:c.1248T>A
|
ENSP00000492096.1:p.Ile416=
|
|
ENST00000640500.1:n.612T>A
|
|
|
ENST00000640739.1:n.6285T>A
|
|
|
ENST00000640910.1:c.776T>A
|
|
|
ENST00000640985.1:c.1251T>A
|
ENSP00000492293.1:p.Ile417=
|
|
ENST00000641017.1:c.1407T>A
|
ENSP00000493461.1:p.Ile469=
|
|
ENST00000356592.7:c.1338T>A
|
ENSP00000349000.3:p.Ile446=
|
|
ENST00000361925.8:c.1314T>A
|
ENSP00000354651.4:p.Ile438=
|
|
ENST00000414552.6:c.1458T>A
|
ENSP00000410732.2:p.Ile486=
|
|
ENST00000522990.5:c.*916T>A
|
ENSP00000430732.1:n.*916T>A
|
|
ENST00000523372.1:c.1435T>A
|
ENSP00000430124.1:n.1435T>A
|
|
NM_000816.3:c.1314T>A
|
NP_000807.2:p.Ile438=
|
|
NM_198903.2:c.1458T>A
|
NP_944493.2:p.Ile486=
|
|
NM_198904.2:c.1338T>A
|
NP_944494.1:p.Ile446=
|
|
NM_001375339.1:c.1329T>A
|
NP_001362268.1:p.Ile443=
|
|
NM_001375340.1:c.*172T>A
|
NP_001362269.1:n.*172T>A
|
|
NM_001375341.1:c.1335T>A
|
NP_001362270.1:p.Ile445=
|
|
NM_001375342.1:c.1311T>A
|
NP_001362271.1:p.Ile437=
|
|
NM_001375343.1:c.1434T>A
|
NP_001362272.1:p.Ile478=
|
|
NM_001375344.1:c.1377T>A
|
NP_001362273.1:p.Ile459=
|
|
NM_001375345.1:c.1248T>A
|
NP_001362274.1:p.Ile416=
|
|
NM_001375346.1:c.1272T>A
|
NP_001362275.1:p.Ile424=
|
|
NM_001375347.1:c.1251T>A
|
NP_001362276.1:p.Ile417=
|
|
NM_001375348.1:c.894T>A
|
NP_001362277.1:p.Ile298=
|
|
NM_001375349.1:c.1029T>A
|
NP_001362278.1:p.Ile343=
|
|
NM_001375350.1:c.918T>A
|
NP_001362279.1:p.Ile306=
|
|
NM_198904.3:c.1338T>A
|
NP_944494.1:p.Ile446=
|
|
NM_198904.4:c.1338T>A
MANE Select
|
NP_944494.1:p.Ile446=
|
|