ENST00000696133.1:c.1289A>T
|
ENSP00000512426.1:p.Asp430Val
|
|
ENST00000696134.1:c.*716A>T
|
ENSP00000512427.1:n.*716A>T
|
|
ENST00000367021.8:c.1289A>T
MANE Select
|
ENSP00000355988.3:p.Asp430Val
|
|
ENST00000643798.1:c.*799A>T
|
ENSP00000496669.1:n.*799A>T
|
|
ENST00000367021.7:c.1289A>T
|
ENSP00000355988.3:p.Asp430Val
|
|
ENST00000542854.5:c.1004A>T
|
ENSP00000440532.1:p.Asp335Val
|
|
NM_001206696.1:c.1004A>T
|
NP_001193625.1:p.Asp335Val
|
|
NM_006147.3:c.1289A>T
|
NP_006138.1:p.Asp430Val
|
|
NM_006147.4:c.1289A>T
MANE Select
|
NP_006138.1:p.Asp430Val
|
|
NM_001206696.2:c.1004A>T
|
NP_001193625.1:p.Asp335Val
|
|