ENST00000481739.2:c.397C>G
MANE Select
|
ENSP00000419692.1:p.His133Asp
|
|
ENST00000672570.1:c.316C>G
|
ENSP00000500402.1:p.His106Asp
|
|
ENST00000356384.4:n.807C>G
|
|
|
ENST00000481739.1:c.397C>G
|
ENSP00000419692.1:p.His133Asp
|
|
NM_001291920.1:c.316C>G
|
NP_001278849.1:p.His106Asp
|
|
NM_001291921.1:c.106C>G
|
NP_001278850.1:p.His36Asp
|
|
NM_002957.5:c.397C>G
|
NP_002948.1:p.His133Asp
|
|
NM_002957.6:c.397C>G
MANE Select
|
NP_002948.1:p.His133Asp
|
|
NM_001291921.2:c.106C>G
|
NP_001278850.1:p.His36Asp
|
|
NM_001291920.2:c.316C>G
|
NP_001278849.1:p.His106Asp
|
|