ENST00000350026.11:c.3924C>T
|
ENSP00000055163.8:p.Asp1308=
|
|
ENST00000414678.8:c.3993C>T
|
ENSP00000412835.3:p.Asp1331=
|
|
ENST00000637015.2:c.4212C>T
|
ENSP00000489729.2:p.Asp1404=
|
|
ENST00000346085.10:c.3963C>T
|
ENSP00000344546.5:p.Asp1321=
|
|
ENST00000350026.10:c.3675C>T
|
ENSP00000055163.7:p.Asp1225=
|
|
ENST00000414678.7:c.2241C>T
|
ENSP00000412835.2:p.Asp747=
|
|
ENST00000635849.1:c.1404C>T
|
ENSP00000490948.1:p.Asp468=
|
|
ENST00000635957.1:c.1035C>T
|
ENSP00000490385.1:p.Asp345=
|
|
ENST00000636930.2:c.4083C>T
MANE Select
|
ENSP00000490491.2:p.Asp1361=
|
|
ENST00000636940.1:n.2080C>T
|
|
|
ENST00000637015.1:c.1451C>T
|
|
|
ENST00000637568.1:c.1365C>T
|
|
|
ENST00000637741.1:n.749C>T
|
|
|
ENST00000637810.1:c.1425C>T
|
ENSP00000489636.1:p.Asp475=
|
|
ENST00000637904.1:c.1584C>T
|
ENSP00000490550.1:p.Asp528=
|
|
ENST00000647938.1:c.3714C>T
|
ENSP00000498155.1:p.Asp1238=
|
|
ENST00000346085.9:c.3714C>T
|
ENSP00000344546.4:p.Asp1238=
|
|
ENST00000350026.9:c.3675C>T
|
ENSP00000055163.7:p.Asp1225=
|
|
ENST00000414678.6:c.2241C>T
|
ENSP00000412835.2:p.Asp747=
|
|
NM_017519.2:c.3675C>T
|
NP_059989.2:p.Asp1225=
|
|
NM_020732.3:c.3714C>T
|
NP_065783.3:p.Asp1238=
|
|
XM_005267069.3:c.3834C>T
|
XP_005267126.2:p.Asp1278=
|
|
XM_011535984.1:c.2913C>T
|
XP_011534286.1:p.Asp971=
|
|
XM_011535985.1:c.2733C>T
|
XP_011534287.1:p.Asp911=
|
|
XM_011535986.1:c.2493C>T
|
XP_011534288.1:p.Asp831=
|
|
XM_011535987.1:c.2112C>T
|
XP_011534289.1:p.Asp704=
|
|
XM_011535988.1:c.975C>T
|
XP_011534290.1:p.Asp325=
|
|
NM_001346813.1:c.3834C>T
|
NP_001333742.1:p.Asp1278=
|
|
NM_001363725.1:c.1584C>T
|
NP_001350654.1:p.Asp528=
|
|
XM_011535984.2:c.4044C>T
|
XP_011534286.2:p.Asp1348=
|
|
XM_011535988.3:c.975C>T
|
XP_011534290.1:p.Asp325=
|
|
XM_017011103.2:c.3945C>T
|
XP_016866592.1:p.Asp1315=
|
|
XM_017011104.1:c.3915C>T
|
XP_016866593.1:p.Asp1305=
|
|
XM_017011105.2:c.3885C>T
|
XP_016866594.1:p.Asp1295=
|
|
XM_017011106.2:c.3756C>T
|
XP_016866595.1:p.Asp1252=
|
|
XM_017011107.2:c.3735C>T
|
XP_016866596.1:p.Asp1245=
|
|
XR_002956289.1:n.4127C>T
|
|
|
NM_001363725.2:c.1584C>T
|
NP_001350654.1:p.Asp528=
|
|
NM_001371656.1:c.3963C>T
|
NP_001358585.1:p.Asp1321=
|
|
NM_001374820.1:c.3963C>T
|
NP_001361749.1:p.Asp1321=
|
|
NM_001374828.1:c.4083C>T
MANE Select
|
NP_001361757.1:p.Asp1361=
|
|
NM_017519.3:c.3924C>T
|
NP_059989.3:p.Asp1308=
|
|