ENST00000481739.2:c.364C>T
MANE Select
|
ENSP00000419692.1:p.His122Tyr
|
|
ENST00000672570.1:c.283C>T
|
ENSP00000500402.1:p.His95Tyr
|
|
ENST00000356384.4:n.774C>T
|
|
|
ENST00000481739.1:c.364C>T
|
ENSP00000419692.1:p.His122Tyr
|
|
NM_001291920.1:c.283C>T
|
NP_001278849.1:p.His95Tyr
|
|
NM_001291921.1:c.73C>T
|
NP_001278850.1:p.His25Tyr
|
|
NM_002957.5:c.364C>T
|
NP_002948.1:p.His122Tyr
|
|
NM_002957.6:c.364C>T
MANE Select
|
NP_002948.1:p.His122Tyr
|
|
NM_001291921.2:c.73C>T
|
NP_001278850.1:p.His25Tyr
|
|
NM_001291920.2:c.283C>T
|
NP_001278849.1:p.His95Tyr
|
|