ENST00000263038.9:c.735G=
MANE Select
|
ENSP00000263038.4:p.Arg245=
|
|
ENST00000263038.8:c.735G=
|
ENSP00000263038.4:p.Arg245=
|
|
ENST00000396913.6:c.435G=
|
ENSP00000380121.2:p.Arg145=
|
|
ENST00000396920.7:c.684G=
|
ENSP00000380126.3:p.Arg228=
|
|
ENST00000453759.6:c.435G=
|
ENSP00000412525.2:p.Arg145=
|
|
NM_001037537.1:c.435G=
|
NP_001032626.1:p.Arg145=
|
|
NM_006214.3:c.735G=
|
NP_006205.1:p.Arg245=
|
|
XM_005252469.2:c.516G=
|
XP_005252526.1:p.Arg172=
|
|
NM_001323080.1:c.435G=
|
NP_001310009.1:p.Arg145=
|
|
NM_001323082.1:c.741G=
|
NP_001310011.1:p.Arg247=
|
|
NM_001323083.1:c.471G=
|
NP_001310012.1:p.Arg157=
|
|
NM_001323084.1:c.441G=
|
NP_001310013.1:p.Arg147=
|
|
NM_006214.4:c.735G=
MANE Select
|
NP_006205.1:p.Arg245=
|
|
NM_001037537.2:c.435G=
|
NP_001032626.1:p.Arg145=
|
|
NM_001323080.2:c.435G=
|
NP_001310009.1:p.Arg145=
|
|
NM_001323082.2:c.741G=
|
NP_001310011.1:p.Arg247=
|
|
NM_001323083.2:c.471G=
|
NP_001310012.1:p.Arg157=
|
|
NM_001323084.2:c.441G=
|
NP_001310013.1:p.Arg147=
|
|