ENST00000481739.2:c.347T>A
MANE Select
|
ENSP00000419692.1:p.Val116Asp
|
|
ENST00000672570.1:c.266T>A
|
ENSP00000500402.1:p.Val89Asp
|
|
ENST00000356384.4:n.757T>A
|
|
|
ENST00000481739.1:c.347T>A
|
ENSP00000419692.1:p.Val116Asp
|
|
NM_001291920.1:c.266T>A
|
NP_001278849.1:p.Val89Asp
|
|
NM_001291921.1:c.56T>A
|
NP_001278850.1:p.Val19Asp
|
|
NM_002957.5:c.347T>A
|
NP_002948.1:p.Val116Asp
|
|
NM_002957.6:c.347T>A
MANE Select
|
NP_002948.1:p.Val116Asp
|
|
NM_001291921.2:c.56T>A
|
NP_001278850.1:p.Val19Asp
|
|
NM_001291920.2:c.266T>A
|
NP_001278849.1:p.Val89Asp
|
|