ENST00000392676.8:c.4262A>T
MANE Select
|
ENSP00000376443.2:p.Asp1421Val
|
|
ENST00000392676.7:c.4262A>T
|
ENSP00000376443.2:p.Asp1421Val
|
|
ENST00000586811.1:c.1160A>T
|
ENSP00000465351.1:p.Asp387Val
|
|
ENST00000586995.5:c.3324A>T
|
ENSP00000467251.1:n.3324A>T
|
|
ENST00000588877.5:c.4262A>T
|
ENSP00000467882.1:p.Asp1421Val
|
|
ENST00000591234.5:c.2204A>T
|
ENSP00000465766.1:n.2204A>T
|
|
NM_018672.4:c.4262A>T
|
NP_061142.2:p.Asp1421Val
|
|
NM_172232.3:c.4262A>T
|
NP_758424.1:p.Asp1421Val
|
|
NM_172232.4:c.4262A>T
MANE Select
|
NP_758424.1:p.Asp1421Val
|
|
NM_018672.5:c.4262A>T
|
NP_061142.2:p.Asp1421Val
|
|