ENST00000350026.11:c.4699G=
|
ENSP00000055163.8:p.Asp1567=
|
|
ENST00000414678.8:c.4768G=
|
ENSP00000412835.3:p.Asp1590=
|
|
ENST00000637015.2:c.4987G=
|
ENSP00000489729.2:p.Asp1663=
|
|
ENST00000346085.10:c.4738G=
|
ENSP00000344546.5:p.Asp1580=
|
|
ENST00000350026.10:c.4450G=
|
ENSP00000055163.7:p.Asp1484=
|
|
ENST00000414678.7:c.3016G=
|
ENSP00000412835.2:p.Asp1006=
|
|
ENST00000635849.1:c.2179G=
|
ENSP00000490948.1:p.Asp727=
|
|
ENST00000635957.1:c.1810G=
|
ENSP00000490385.1:p.Asp604=
|
|
ENST00000636227.1:n.3321G=
|
|
|
ENST00000636254.1:n.778G=
|
|
|
ENST00000636930.2:c.4858G=
MANE Select
|
ENSP00000490491.2:p.Asp1620=
|
|
ENST00000636940.1:n.2855G=
|
|
|
ENST00000637015.1:c.2226G=
|
|
|
ENST00000637568.1:c.2140G=
|
|
|
ENST00000637741.1:n.1524G=
|
|
|
ENST00000637810.1:c.2200G=
|
ENSP00000489636.1:p.Asp734=
|
|
ENST00000637904.1:c.2359G=
|
ENSP00000490550.1:p.Asp787=
|
|
ENST00000647938.1:c.4489G=
|
ENSP00000498155.1:p.Asp1497=
|
|
ENST00000346085.9:c.4489G=
|
ENSP00000344546.4:p.Asp1497=
|
|
ENST00000350026.9:c.4450G=
|
ENSP00000055163.7:p.Asp1484=
|
|
ENST00000414678.6:c.3016G=
|
ENSP00000412835.2:p.Asp1006=
|
|
NM_017519.2:c.4450G=
|
NP_059989.2:p.Asp1484=
|
|
NM_020732.3:c.4489G=
|
NP_065783.3:p.Asp1497=
|
|
XM_005267069.3:c.4609G=
|
XP_005267126.2:p.Asp1537=
|
|
XM_011535984.1:c.3688G=
|
XP_011534286.1:p.Asp1230=
|
|
XM_011535985.1:c.3508G=
|
XP_011534287.1:p.Asp1170=
|
|
XM_011535986.1:c.3268G=
|
XP_011534288.1:p.Asp1090=
|
|
XM_011535987.1:c.2887G=
|
XP_011534289.1:p.Asp963=
|
|
XM_011535988.1:c.1750G=
|
XP_011534290.1:p.Asp584=
|
|
NM_001346813.1:c.4609G=
|
NP_001333742.1:p.Asp1537=
|
|
NM_001363725.1:c.2359G=
|
NP_001350654.1:p.Asp787=
|
|
XM_011535984.2:c.4819G=
|
XP_011534286.2:p.Asp1607=
|
|
XM_011535988.3:c.1750G=
|
XP_011534290.1:p.Asp584=
|
|
XM_017011103.2:c.4720G=
|
XP_016866592.1:p.Asp1574=
|
|
XM_017011104.1:c.4690G=
|
XP_016866593.1:p.Asp1564=
|
|
XM_017011105.2:c.4660G=
|
XP_016866594.1:p.Asp1554=
|
|
XM_017011106.2:c.4531G=
|
XP_016866595.1:p.Asp1511=
|
|
XM_017011107.2:c.4510G=
|
XP_016866596.1:p.Asp1504=
|
|
XR_002956289.1:n.4805G=
|
|
|
NM_001363725.2:c.2359G=
|
NP_001350654.1:p.Asp787=
|
|
NM_001371656.1:c.4738G=
|
NP_001358585.1:p.Asp1580=
|
|
NM_001374820.1:c.4738G=
|
NP_001361749.1:p.Asp1580=
|
|
NM_001374828.1:c.4858G=
MANE Select
|
NP_001361757.1:p.Asp1620=
|
|
NM_017519.3:c.4699G=
|
NP_059989.3:p.Asp1567=
|
|