ENST00000350026.11:c.3934G>C
|
ENSP00000055163.8:p.Asp1312His
|
|
ENST00000414678.8:c.4003G>C
|
ENSP00000412835.3:p.Asp1335His
|
|
ENST00000637015.2:c.4222G>C
|
ENSP00000489729.2:p.Asp1408His
|
|
ENST00000346085.10:c.3973G>C
|
ENSP00000344546.5:p.Asp1325His
|
|
ENST00000350026.10:c.3685G>C
|
ENSP00000055163.7:p.Asp1229His
|
|
ENST00000414678.7:c.2251G>C
|
ENSP00000412835.2:p.Asp751His
|
|
ENST00000635849.1:c.1414G>C
|
ENSP00000490948.1:p.Asp472His
|
|
ENST00000635957.1:c.1045G>C
|
ENSP00000490385.1:p.Asp349His
|
|
ENST00000636930.2:c.4093G>C
MANE Select
|
ENSP00000490491.2:p.Asp1365His
|
|
ENST00000636940.1:n.2090G>C
|
|
|
ENST00000637015.1:c.1461G>C
|
|
|
ENST00000637568.1:c.1375G>C
|
|
|
ENST00000637741.1:n.759G>C
|
|
|
ENST00000637810.1:c.1435G>C
|
ENSP00000489636.1:p.Asp479His
|
|
ENST00000637904.1:c.1594G>C
|
ENSP00000490550.1:p.Asp532His
|
|
ENST00000647938.1:c.3724G>C
|
ENSP00000498155.1:p.Asp1242His
|
|
ENST00000346085.9:c.3724G>C
|
ENSP00000344546.4:p.Asp1242His
|
|
ENST00000350026.9:c.3685G>C
|
ENSP00000055163.7:p.Asp1229His
|
|
ENST00000414678.6:c.2251G>C
|
ENSP00000412835.2:p.Asp751His
|
|
NM_017519.2:c.3685G>C
|
NP_059989.2:p.Asp1229His
|
|
NM_020732.3:c.3724G>C
|
NP_065783.3:p.Asp1242His
|
|
XM_005267069.3:c.3844G>C
|
XP_005267126.2:p.Asp1282His
|
|
XM_011535984.1:c.2923G>C
|
XP_011534286.1:p.Asp975His
|
|
XM_011535985.1:c.2743G>C
|
XP_011534287.1:p.Asp915His
|
|
XM_011535986.1:c.2503G>C
|
XP_011534288.1:p.Asp835His
|
|
XM_011535987.1:c.2122G>C
|
XP_011534289.1:p.Asp708His
|
|
XM_011535988.1:c.985G>C
|
XP_011534290.1:p.Asp329His
|
|
NM_001346813.1:c.3844G>C
|
NP_001333742.1:p.Asp1282His
|
|
NM_001363725.1:c.1594G>C
|
NP_001350654.1:p.Asp532His
|
|
XM_011535984.2:c.4054G>C
|
XP_011534286.2:p.Asp1352His
|
|
XM_011535988.3:c.985G>C
|
XP_011534290.1:p.Asp329His
|
|
XM_017011103.2:c.3955G>C
|
XP_016866592.1:p.Asp1319His
|
|
XM_017011104.1:c.3925G>C
|
XP_016866593.1:p.Asp1309His
|
|
XM_017011105.2:c.3895G>C
|
XP_016866594.1:p.Asp1299His
|
|
XM_017011106.2:c.3766G>C
|
XP_016866595.1:p.Asp1256His
|
|
XM_017011107.2:c.3745G>C
|
XP_016866596.1:p.Asp1249His
|
|
XR_002956289.1:n.4137G>C
|
|
|
NM_001363725.2:c.1594G>C
|
NP_001350654.1:p.Asp532His
|
|
NM_001371656.1:c.3973G>C
|
NP_001358585.1:p.Asp1325His
|
|
NM_001374820.1:c.3973G>C
|
NP_001361749.1:p.Asp1325His
|
|
NM_001374828.1:c.4093G>C
MANE Select
|
NP_001361757.1:p.Asp1365His
|
|
NM_017519.3:c.3934G>C
|
NP_059989.3:p.Asp1312His
|
|