ENST00000481739.2:c.413G>A
MANE Select
|
ENSP00000419692.1:p.Cys138Tyr
|
|
ENST00000672570.1:c.332G>A
|
ENSP00000500402.1:p.Cys111Tyr
|
|
ENST00000356384.4:n.823G>A
|
|
|
ENST00000481739.1:c.413G>A
|
ENSP00000419692.1:p.Cys138Tyr
|
|
NM_001291920.1:c.332G>A
|
NP_001278849.1:p.Cys111Tyr
|
|
NM_001291921.1:c.122G>A
|
NP_001278850.1:p.Cys41Tyr
|
|
NM_002957.5:c.413G>A
|
NP_002948.1:p.Cys138Tyr
|
|
NM_002957.6:c.413G>A
MANE Select
|
NP_002948.1:p.Cys138Tyr
|
|
NM_001291921.2:c.122G>A
|
NP_001278850.1:p.Cys41Tyr
|
|
NM_001291920.2:c.332G>A
|
NP_001278849.1:p.Cys111Tyr
|
|