ENST00000251102.13:c.2763C>G
MANE Select
|
ENSP00000251102.8:p.Tyr921Ter
|
|
ENST00000251102.12:c.2763C>G
|
ENSP00000251102.8:p.Tyr921Ter
|
|
ENST00000564448.5:c.2745C>G
|
ENSP00000454633.1:p.Tyr915Ter
|
|
ENST00000569643.1:n.420C>G
|
|
|
NM_001286130.1:c.2745C>G
|
NP_001273059.1:p.Tyr915Ter
|
|
NM_001297.4:c.2763C>G
|
NP_001288.3:p.Tyr921Ter
|
|
XM_006721134.2:c.2763C>G
|
XP_006721197.1:p.Tyr921Ter
|
|
XM_011522870.1:c.1614C>G
|
XP_011521172.1:p.Tyr538Ter
|
|
XM_011522870.2:c.1614C>G
|
XP_011521172.1:p.Tyr538Ter
|
|
NM_001286130.2:c.2745C>G
|
NP_001273059.1:p.Tyr915Ter
|
|
NM_001297.5:c.2763C>G
MANE Select
|
NP_001288.3:p.Tyr921Ter
|
|