ENST00000350026.11:c.4668G>C
|
ENSP00000055163.8:p.Gln1556His
|
|
ENST00000414678.8:c.4737G>C
|
ENSP00000412835.3:p.Gln1579His
|
|
ENST00000637015.2:c.4956G>C
|
ENSP00000489729.2:p.Gln1652His
|
|
ENST00000346085.10:c.4707G>C
|
ENSP00000344546.5:p.Gln1569His
|
|
ENST00000350026.10:c.4419G>C
|
ENSP00000055163.7:p.Gln1473His
|
|
ENST00000414678.7:c.2985G>C
|
ENSP00000412835.2:p.Gln995His
|
|
ENST00000635849.1:c.2148G>C
|
ENSP00000490948.1:p.Gln716His
|
|
ENST00000635957.1:c.1779G>C
|
ENSP00000490385.1:p.Gln593His
|
|
ENST00000636227.1:n.3290G>C
|
|
|
ENST00000636254.1:n.747G>C
|
|
|
ENST00000636930.2:c.4827G>C
MANE Select
|
ENSP00000490491.2:p.Gln1609His
|
|
ENST00000636940.1:n.2824G>C
|
|
|
ENST00000637015.1:c.2195G>C
|
|
|
ENST00000637568.1:c.2109G>C
|
|
|
ENST00000637741.1:n.1493G>C
|
|
|
ENST00000637810.1:c.2169G>C
|
ENSP00000489636.1:p.Gln723His
|
|
ENST00000637904.1:c.2328G>C
|
ENSP00000490550.1:p.Gln776His
|
|
ENST00000647938.1:c.4458G>C
|
ENSP00000498155.1:p.Gln1486His
|
|
ENST00000346085.9:c.4458G>C
|
ENSP00000344546.4:p.Gln1486His
|
|
ENST00000350026.9:c.4419G>C
|
ENSP00000055163.7:p.Gln1473His
|
|
ENST00000414678.6:c.2985G>C
|
ENSP00000412835.2:p.Gln995His
|
|
NM_017519.2:c.4419G>C
|
NP_059989.2:p.Gln1473His
|
|
NM_020732.3:c.4458G>C
|
NP_065783.3:p.Gln1486His
|
|
XM_005267069.3:c.4578G>C
|
XP_005267126.2:p.Gln1526His
|
|
XM_011535984.1:c.3657G>C
|
XP_011534286.1:p.Gln1219His
|
|
XM_011535985.1:c.3477G>C
|
XP_011534287.1:p.Gln1159His
|
|
XM_011535986.1:c.3237G>C
|
XP_011534288.1:p.Gln1079His
|
|
XM_011535987.1:c.2856G>C
|
XP_011534289.1:p.Gln952His
|
|
XM_011535988.1:c.1719G>C
|
XP_011534290.1:p.Gln573His
|
|
NM_001346813.1:c.4578G>C
|
NP_001333742.1:p.Gln1526His
|
|
NM_001363725.1:c.2328G>C
|
NP_001350654.1:p.Gln776His
|
|
XM_011535984.2:c.4788G>C
|
XP_011534286.2:p.Gln1596His
|
|
XM_011535988.3:c.1719G>C
|
XP_011534290.1:p.Gln573His
|
|
XM_017011103.2:c.4689G>C
|
XP_016866592.1:p.Gln1563His
|
|
XM_017011104.1:c.4659G>C
|
XP_016866593.1:p.Gln1553His
|
|
XM_017011105.2:c.4629G>C
|
XP_016866594.1:p.Gln1543His
|
|
XM_017011106.2:c.4500G>C
|
XP_016866595.1:p.Gln1500His
|
|
XM_017011107.2:c.4479G>C
|
XP_016866596.1:p.Gln1493His
|
|
XR_002956289.1:n.4774G>C
|
|
|
NM_001363725.2:c.2328G>C
|
NP_001350654.1:p.Gln776His
|
|
NM_001371656.1:c.4707G>C
|
NP_001358585.1:p.Gln1569His
|
|
NM_001374820.1:c.4707G>C
|
NP_001361749.1:p.Gln1569His
|
|
NM_001374828.1:c.4827G>C
MANE Select
|
NP_001361757.1:p.Gln1609His
|
|
NM_017519.3:c.4668G>C
|
NP_059989.3:p.Gln1556His
|
|