ENST00000350026.11:c.4695C>A
|
ENSP00000055163.8:p.Arg1565=
|
|
ENST00000414678.8:c.4764C>A
|
ENSP00000412835.3:p.Arg1588=
|
|
ENST00000637015.2:c.4983C>A
|
ENSP00000489729.2:p.Arg1661=
|
|
ENST00000346085.10:c.4734C>A
|
ENSP00000344546.5:p.Arg1578=
|
|
ENST00000350026.10:c.4446C>A
|
ENSP00000055163.7:p.Arg1482=
|
|
ENST00000414678.7:c.3012C>A
|
ENSP00000412835.2:p.Arg1004=
|
|
ENST00000635849.1:c.2175C>A
|
ENSP00000490948.1:p.Arg725=
|
|
ENST00000635957.1:c.1806C>A
|
ENSP00000490385.1:p.Arg602=
|
|
ENST00000636227.1:n.3317C>A
|
|
|
ENST00000636254.1:n.774C>A
|
|
|
ENST00000636930.2:c.4854C>A
MANE Select
|
ENSP00000490491.2:p.Arg1618=
|
|
ENST00000636940.1:n.2851C>A
|
|
|
ENST00000637015.1:c.2222C>A
|
|
|
ENST00000637568.1:c.2136C>A
|
|
|
ENST00000637741.1:n.1520C>A
|
|
|
ENST00000637810.1:c.2196C>A
|
ENSP00000489636.1:p.Arg732=
|
|
ENST00000637904.1:c.2355C>A
|
ENSP00000490550.1:p.Arg785=
|
|
ENST00000647938.1:c.4485C>A
|
ENSP00000498155.1:p.Arg1495=
|
|
ENST00000346085.9:c.4485C>A
|
ENSP00000344546.4:p.Arg1495=
|
|
ENST00000350026.9:c.4446C>A
|
ENSP00000055163.7:p.Arg1482=
|
|
ENST00000414678.6:c.3012C>A
|
ENSP00000412835.2:p.Arg1004=
|
|
NM_017519.2:c.4446C>A
|
NP_059989.2:p.Arg1482=
|
|
NM_020732.3:c.4485C>A
|
NP_065783.3:p.Arg1495=
|
|
XM_005267069.3:c.4605C>A
|
XP_005267126.2:p.Arg1535=
|
|
XM_011535984.1:c.3684C>A
|
XP_011534286.1:p.Arg1228=
|
|
XM_011535985.1:c.3504C>A
|
XP_011534287.1:p.Arg1168=
|
|
XM_011535986.1:c.3264C>A
|
XP_011534288.1:p.Arg1088=
|
|
XM_011535987.1:c.2883C>A
|
XP_011534289.1:p.Arg961=
|
|
XM_011535988.1:c.1746C>A
|
XP_011534290.1:p.Arg582=
|
|
NM_001346813.1:c.4605C>A
|
NP_001333742.1:p.Arg1535=
|
|
NM_001363725.1:c.2355C>A
|
NP_001350654.1:p.Arg785=
|
|
XM_011535984.2:c.4815C>A
|
XP_011534286.2:p.Arg1605=
|
|
XM_011535988.3:c.1746C>A
|
XP_011534290.1:p.Arg582=
|
|
XM_017011103.2:c.4716C>A
|
XP_016866592.1:p.Arg1572=
|
|
XM_017011104.1:c.4686C>A
|
XP_016866593.1:p.Arg1562=
|
|
XM_017011105.2:c.4656C>A
|
XP_016866594.1:p.Arg1552=
|
|
XM_017011106.2:c.4527C>A
|
XP_016866595.1:p.Arg1509=
|
|
XM_017011107.2:c.4506C>A
|
XP_016866596.1:p.Arg1502=
|
|
XR_002956289.1:n.4801C>A
|
|
|
NM_001363725.2:c.2355C>A
|
NP_001350654.1:p.Arg785=
|
|
NM_001371656.1:c.4734C>A
|
NP_001358585.1:p.Arg1578=
|
|
NM_001374820.1:c.4734C>A
|
NP_001361749.1:p.Arg1578=
|
|
NM_001374828.1:c.4854C>A
MANE Select
|
NP_001361757.1:p.Arg1618=
|
|
NM_017519.3:c.4695C>A
|
NP_059989.3:p.Arg1565=
|
|