ENST00000481739.2:c.427T>A
MANE Select
|
ENSP00000419692.1:p.Ser143Thr
|
|
ENST00000672570.1:c.346T>A
|
ENSP00000500402.1:p.Ser116Thr
|
|
ENST00000356384.4:n.837T>A
|
|
|
ENST00000481739.1:c.427T>A
|
ENSP00000419692.1:p.Ser143Thr
|
|
NM_001291920.1:c.346T>A
|
NP_001278849.1:p.Ser116Thr
|
|
NM_001291921.1:c.136T>A
|
NP_001278850.1:p.Ser46Thr
|
|
NM_002957.5:c.427T>A
|
NP_002948.1:p.Ser143Thr
|
|
NM_002957.6:c.427T>A
MANE Select
|
NP_002948.1:p.Ser143Thr
|
|
NM_001291921.2:c.136T>A
|
NP_001278850.1:p.Ser46Thr
|
|
NM_001291920.2:c.346T>A
|
NP_001278849.1:p.Ser116Thr
|
|