ENST00000350026.11:c.4582G=
|
ENSP00000055163.8:p.Glu1528=
|
|
ENST00000414678.8:c.4651G=
|
ENSP00000412835.3:p.Glu1551=
|
|
ENST00000637015.2:c.4870G=
|
ENSP00000489729.2:p.Glu1624=
|
|
ENST00000346085.10:c.4621G=
|
ENSP00000344546.5:p.Glu1541=
|
|
ENST00000350026.10:c.4333G=
|
ENSP00000055163.7:p.Glu1445=
|
|
ENST00000414678.7:c.2899G=
|
ENSP00000412835.2:p.Glu967=
|
|
ENST00000635849.1:c.2062G=
|
ENSP00000490948.1:p.Glu688=
|
|
ENST00000635957.1:c.1693G=
|
ENSP00000490385.1:p.Glu565=
|
|
ENST00000636227.1:n.3204G=
|
|
|
ENST00000636254.1:n.661G=
|
|
|
ENST00000636930.2:c.4741G=
MANE Select
|
ENSP00000490491.2:p.Glu1581=
|
|
ENST00000636940.1:n.2738G=
|
|
|
ENST00000637015.1:c.2109G=
|
|
|
ENST00000637568.1:c.2023G=
|
|
|
ENST00000637741.1:n.1407G=
|
|
|
ENST00000637810.1:c.2083G=
|
ENSP00000489636.1:p.Glu695=
|
|
ENST00000637904.1:c.2242G=
|
ENSP00000490550.1:p.Glu748=
|
|
ENST00000647938.1:c.4372G=
|
ENSP00000498155.1:p.Glu1458=
|
|
ENST00000346085.9:c.4372G=
|
ENSP00000344546.4:p.Glu1458=
|
|
ENST00000350026.9:c.4333G=
|
ENSP00000055163.7:p.Glu1445=
|
|
ENST00000414678.6:c.2899G=
|
ENSP00000412835.2:p.Glu967=
|
|
NM_017519.2:c.4333G=
|
NP_059989.2:p.Glu1445=
|
|
NM_020732.3:c.4372G=
|
NP_065783.3:p.Glu1458=
|
|
XM_005267069.3:c.4492G=
|
XP_005267126.2:p.Glu1498=
|
|
XM_011535984.1:c.3571G=
|
XP_011534286.1:p.Glu1191=
|
|
XM_011535985.1:c.3391G=
|
XP_011534287.1:p.Glu1131=
|
|
XM_011535986.1:c.3151G=
|
XP_011534288.1:p.Glu1051=
|
|
XM_011535987.1:c.2770G=
|
XP_011534289.1:p.Glu924=
|
|
XM_011535988.1:c.1633G=
|
XP_011534290.1:p.Glu545=
|
|
NM_001346813.1:c.4492G=
|
NP_001333742.1:p.Glu1498=
|
|
NM_001363725.1:c.2242G=
|
NP_001350654.1:p.Glu748=
|
|
XM_011535984.2:c.4702G=
|
XP_011534286.2:p.Glu1568=
|
|
XM_011535988.3:c.1633G=
|
XP_011534290.1:p.Glu545=
|
|
XM_017011103.2:c.4603G=
|
XP_016866592.1:p.Glu1535=
|
|
XM_017011104.1:c.4573G=
|
XP_016866593.1:p.Glu1525=
|
|
XM_017011105.2:c.4543G=
|
XP_016866594.1:p.Glu1515=
|
|
XM_017011106.2:c.4414G=
|
XP_016866595.1:p.Glu1472=
|
|
XM_017011107.2:c.4393G=
|
XP_016866596.1:p.Glu1465=
|
|
XR_002956289.1:n.4688G=
|
|
|
NM_001363725.2:c.2242G=
|
NP_001350654.1:p.Glu748=
|
|
NM_001371656.1:c.4621G=
|
NP_001358585.1:p.Glu1541=
|
|
NM_001374820.1:c.4621G=
|
NP_001361749.1:p.Glu1541=
|
|
NM_001374828.1:c.4741G=
MANE Select
|
NP_001361757.1:p.Glu1581=
|
|
NM_017519.3:c.4582G=
|
NP_059989.3:p.Glu1528=
|
|