ENST00000267622.8:c.4727G>A
MANE Select
|
ENSP00000267622.4:p.Arg1576His
|
|
ENST00000554357.5:c.3873G>A
|
|
|
NM_004239.3:c.4727G>A
|
NP_004230.2:p.Arg1576His
|
|
XM_005268214.2:c.3401G>A
|
XP_005268271.1:p.Arg1134His
|
|
XM_005268215.2:c.1697G>A
|
XP_005268272.1:p.Arg566His
|
|
XM_006720321.2:c.4724G>A
|
XP_006720384.1:p.Arg1575His
|
|
XM_011537361.1:c.4727G>A
|
XP_011535663.1:p.Arg1576His
|
|
XR_943560.1:n.5182G>A
|
|
|
NM_001321851.1:c.4724G>A
|
NP_001308780.1:p.Arg1575His
|
|
NM_004239.4:c.4727G>A
MANE Select
|
NP_004230.2:p.Arg1576His
|
|
XM_017021787.2:c.4022G>A
|
XP_016877276.1:p.Arg1341His
|
|
XM_017021788.2:c.3401G>A
|
XP_016877277.1:p.Arg1134His
|
|
XR_001750598.2:n.5176G>A
|
|
|
XR_943560.2:n.5176G>A
|
|
|