ENST00000414306.6:c.*468A>T
|
ENSP00000394586.1:n.*468A>T
|
|
ENST00000697860.1:n.704A>T
|
|
|
ENST00000697861.1:c.536A>T
|
ENSP00000513460.1:p.Asp179Val
|
|
ENST00000697862.1:c.*178A>T
|
ENSP00000513461.1:n.*178A>T
|
|
ENST00000697863.1:c.680A>T
|
ENSP00000513462.1:p.Asp227Val
|
|
ENST00000697864.1:n.1881A>T
|
|
|
ENST00000697865.1:c.680A>T
|
ENSP00000513463.1:p.Asp227Val
|
|
ENST00000697866.1:c.419A>T
|
ENSP00000513464.1:p.Asp140Val
|
|
ENST00000697867.1:c.715A>T
|
|
|
ENST00000697868.1:c.*501A>T
|
ENSP00000513466.1:n.*501A>T
|
|
ENST00000697897.1:c.737A>T
|
ENSP00000513469.1:p.Asp246Val
|
|
ENST00000246868.7:c.737A>T
MANE Select
|
ENSP00000246868.2:p.Asp246Val
|
|
ENST00000246868.6:c.737A>T
|
ENSP00000246868.2:p.Asp246Val
|
|
ENST00000414306.5:c.*468A>T
|
ENSP00000394586.1:n.*468A>T
|
|
ENST00000617799.1:c.737A>T
|
ENSP00000483040.1:p.Asp246Val
|
|
NM_016038.2:c.737A>T , LRG_104t1:c.737A>T
|
NP_057122.2:p.Asp246Val
|
|
NM_016038.3:c.737A>T
|
NP_057122.2:p.Asp246Val
|
|
NM_016038.4:c.737A>T
MANE Select
|
NP_057122.2:p.Asp246Val
|
|