ENST00000481739.2:c.380T>G
MANE Select
|
ENSP00000419692.1:p.Met127Arg
|
|
ENST00000672570.1:c.299T>G
|
ENSP00000500402.1:p.Met100Arg
|
|
ENST00000356384.4:n.790T>G
|
|
|
ENST00000481739.1:c.380T>G
|
ENSP00000419692.1:p.Met127Arg
|
|
NM_001291920.1:c.299T>G
|
NP_001278849.1:p.Met100Arg
|
|
NM_001291921.1:c.89T>G
|
NP_001278850.1:p.Met30Arg
|
|
NM_002957.5:c.380T>G
|
NP_002948.1:p.Met127Arg
|
|
NM_002957.6:c.380T>G
MANE Select
|
NP_002948.1:p.Met127Arg
|
|
NM_001291921.2:c.89T>G
|
NP_001278850.1:p.Met30Arg
|
|
NM_001291920.2:c.299T>G
|
NP_001278849.1:p.Met100Arg
|
|