ENST00000393716.8:c.56A>T
MANE Select
|
ENSP00000377319.3:p.Asp19Val
|
|
ENST00000466380.6:c.56A>T
|
ENSP00000420297.2:p.Asp19Val
|
|
ENST00000648112.1:c.*79A>T
|
ENSP00000497876.1:n.*79A>T
|
|
ENST00000337940.4:c.173A>T
|
ENSP00000336528.4:p.Asp58Val
|
|
ENST00000393716.6:c.56A>T
|
ENSP00000377319.2:p.Asp19Val
|
|
ENST00000466380.5:c.56A>T
|
ENSP00000420297.1:p.Asp19Val
|
|
ENST00000474090.1:n.344A>T
|
|
|
NM_003889.3:c.56A>T
|
NP_003880.3:p.Asp19Val
|
|
NM_022002.2:c.173A>T
|
NP_071285.1:p.Asp58Val
|
|
NM_033013.2:c.56A>T
|
NP_148934.1:p.Asp19Val
|
|
NM_003889.4:c.56A>T
MANE Select
|
NP_003880.3:p.Asp19Val
|
|
NM_022002.3:c.173A>T
|
NP_071285.1:p.Asp58Val
|
|
NM_033013.3:c.56A>T
|
NP_148934.1:p.Asp19Val
|
|