ENST00000350026.11:c.4668G>A
|
ENSP00000055163.8:p.Gln1556=
|
|
ENST00000414678.8:c.4737G>A
|
ENSP00000412835.3:p.Gln1579=
|
|
ENST00000637015.2:c.4956G>A
|
ENSP00000489729.2:p.Gln1652=
|
|
ENST00000346085.10:c.4707G>A
|
ENSP00000344546.5:p.Gln1569=
|
|
ENST00000350026.10:c.4419G>A
|
ENSP00000055163.7:p.Gln1473=
|
|
ENST00000414678.7:c.2985G>A
|
ENSP00000412835.2:p.Gln995=
|
|
ENST00000635849.1:c.2148G>A
|
ENSP00000490948.1:p.Gln716=
|
|
ENST00000635957.1:c.1779G>A
|
ENSP00000490385.1:p.Gln593=
|
|
ENST00000636227.1:n.3290G>A
|
|
|
ENST00000636254.1:n.747G>A
|
|
|
ENST00000636930.2:c.4827G>A
MANE Select
|
ENSP00000490491.2:p.Gln1609=
|
|
ENST00000636940.1:n.2824G>A
|
|
|
ENST00000637015.1:c.2195G>A
|
|
|
ENST00000637568.1:c.2109G>A
|
|
|
ENST00000637741.1:n.1493G>A
|
|
|
ENST00000637810.1:c.2169G>A
|
ENSP00000489636.1:p.Gln723=
|
|
ENST00000637904.1:c.2328G>A
|
ENSP00000490550.1:p.Gln776=
|
|
ENST00000647938.1:c.4458G>A
|
ENSP00000498155.1:p.Gln1486=
|
|
ENST00000346085.9:c.4458G>A
|
ENSP00000344546.4:p.Gln1486=
|
|
ENST00000350026.9:c.4419G>A
|
ENSP00000055163.7:p.Gln1473=
|
|
ENST00000414678.6:c.2985G>A
|
ENSP00000412835.2:p.Gln995=
|
|
NM_017519.2:c.4419G>A
|
NP_059989.2:p.Gln1473=
|
|
NM_020732.3:c.4458G>A
|
NP_065783.3:p.Gln1486=
|
|
XM_005267069.3:c.4578G>A
|
XP_005267126.2:p.Gln1526=
|
|
XM_011535984.1:c.3657G>A
|
XP_011534286.1:p.Gln1219=
|
|
XM_011535985.1:c.3477G>A
|
XP_011534287.1:p.Gln1159=
|
|
XM_011535986.1:c.3237G>A
|
XP_011534288.1:p.Gln1079=
|
|
XM_011535987.1:c.2856G>A
|
XP_011534289.1:p.Gln952=
|
|
XM_011535988.1:c.1719G>A
|
XP_011534290.1:p.Gln573=
|
|
NM_001346813.1:c.4578G>A
|
NP_001333742.1:p.Gln1526=
|
|
NM_001363725.1:c.2328G>A
|
NP_001350654.1:p.Gln776=
|
|
XM_011535984.2:c.4788G>A
|
XP_011534286.2:p.Gln1596=
|
|
XM_011535988.3:c.1719G>A
|
XP_011534290.1:p.Gln573=
|
|
XM_017011103.2:c.4689G>A
|
XP_016866592.1:p.Gln1563=
|
|
XM_017011104.1:c.4659G>A
|
XP_016866593.1:p.Gln1553=
|
|
XM_017011105.2:c.4629G>A
|
XP_016866594.1:p.Gln1543=
|
|
XM_017011106.2:c.4500G>A
|
XP_016866595.1:p.Gln1500=
|
|
XM_017011107.2:c.4479G>A
|
XP_016866596.1:p.Gln1493=
|
|
XR_002956289.1:n.4774G>A
|
|
|
NM_001363725.2:c.2328G>A
|
NP_001350654.1:p.Gln776=
|
|
NM_001371656.1:c.4707G>A
|
NP_001358585.1:p.Gln1569=
|
|
NM_001374820.1:c.4707G>A
|
NP_001361749.1:p.Gln1569=
|
|
NM_001374828.1:c.4827G>A
MANE Select
|
NP_001361757.1:p.Gln1609=
|
|
NM_017519.3:c.4668G>A
|
NP_059989.3:p.Gln1556=
|
|