ENST00000356592.8:c.1314G>C
|
|
|
ENST00000361925.9:c.1409G>C
|
ENSP00000354651.5:p.Arg470Thr
|
|
ENST00000523372.2:c.1372G>C
|
|
|
ENST00000638253.1:n.567G>C
|
|
|
ENST00000638552.1:c.1004G>C
|
ENSP00000491763.1:p.Arg335Thr
|
|
ENST00000638660.1:c.1028G>C
|
ENSP00000492869.1:p.Arg343Thr
|
|
ENST00000638772.1:c.*3910G>C
|
ENSP00000491557.1:n.*3910G>C
|
|
ENST00000638877.1:c.1190G>C
|
|
|
ENST00000639046.1:c.680G>C
|
ENSP00000492659.1:p.Arg227Thr
|
|
ENST00000639111.2:c.1289G>C
|
ENSP00000492125.2:p.Arg430Thr
|
|
ENST00000639213.2:c.1313G>C
MANE Select
|
ENSP00000491909.2:p.Arg438Thr
|
|
ENST00000639278.1:c.1976G>C
|
ENSP00000491958.1:n.1976G>C
|
|
ENST00000639384.1:c.*1494G>C
|
ENSP00000491240.1:n.*1494G>C
|
|
ENST00000639424.1:c.*513G>C
|
ENSP00000491245.1:n.*513G>C
|
|
ENST00000639683.1:c.1247G>C
|
ENSP00000492581.1:p.Arg416Thr
|
|
ENST00000639975.1:c.1223G>C
|
ENSP00000492096.1:p.Arg408Thr
|
|
ENST00000640500.1:n.587G>C
|
|
|
ENST00000640739.1:n.6260G>C
|
|
|
ENST00000640910.1:c.751G>C
|
|
|
ENST00000640985.1:c.1226G>C
|
ENSP00000492293.1:p.Arg409Thr
|
|
ENST00000641017.1:c.1382G>C
|
ENSP00000493461.1:p.Arg461Thr
|
|
ENST00000356592.7:c.1313G>C
|
ENSP00000349000.3:p.Arg438Thr
|
|
ENST00000361925.8:c.1289G>C
|
ENSP00000354651.4:p.Arg430Thr
|
|
ENST00000414552.6:c.1433G>C
|
ENSP00000410732.2:p.Arg478Thr
|
|
ENST00000522990.5:c.*891G>C
|
ENSP00000430732.1:n.*891G>C
|
|
ENST00000523372.1:c.1410G>C
|
ENSP00000430124.1:n.1410G>C
|
|
NM_000816.3:c.1289G>C
|
NP_000807.2:p.Arg430Thr
|
|
NM_198903.2:c.1433G>C
|
NP_944493.2:p.Arg478Thr
|
|
NM_198904.2:c.1313G>C
|
NP_944494.1:p.Arg438Thr
|
|
NM_001375339.1:c.1304G>C
|
NP_001362268.1:p.Arg435Thr
|
|
NM_001375340.1:c.*147G>C
|
NP_001362269.1:n.*147G>C
|
|
NM_001375341.1:c.1310G>C
|
NP_001362270.1:p.Arg437Thr
|
|
NM_001375342.1:c.1286G>C
|
NP_001362271.1:p.Arg429Thr
|
|
NM_001375343.1:c.1409G>C
|
NP_001362272.1:p.Arg470Thr
|
|
NM_001375344.1:c.1352G>C
|
NP_001362273.1:p.Arg451Thr
|
|
NM_001375345.1:c.1223G>C
|
NP_001362274.1:p.Arg408Thr
|
|
NM_001375346.1:c.1247G>C
|
NP_001362275.1:p.Arg416Thr
|
|
NM_001375347.1:c.1226G>C
|
NP_001362276.1:p.Arg409Thr
|
|
NM_001375348.1:c.869G>C
|
NP_001362277.1:p.Arg290Thr
|
|
NM_001375349.1:c.1004G>C
|
NP_001362278.1:p.Arg335Thr
|
|
NM_001375350.1:c.893G>C
|
NP_001362279.1:p.Arg298Thr
|
|
NM_198904.3:c.1313G>C
|
NP_944494.1:p.Arg438Thr
|
|
NM_198904.4:c.1313G>C
MANE Select
|
NP_944494.1:p.Arg438Thr
|
|