ENST00000269980.7:c.1283C>A
MANE Select
|
ENSP00000269980.2:p.Ala428Asp
|
|
ENST00000269980.6:c.1283C>A
|
ENSP00000269980.2:p.Ala428Asp
|
|
ENST00000457836.6:c.1292C>A
|
ENSP00000416000.2:p.Ala431Asp
|
|
ENST00000540732.3:c.1385C>A
|
ENSP00000443246.1:p.Ala462Asp
|
|
ENST00000544905.1:c.113C>A
|
|
|
ENST00000595085.5:c.922+1856C>A
|
ENSP00000471150.2:n.922+1856C>A
|
|
NM_000709.3:c.1283C>A
|
NP_000700.1:p.Ala428Asp
|
|
NM_001164783.1:c.1280C>A
|
NP_001158255.1:p.Ala427Asp
|
|
NM_000709.4:c.1283C>A
MANE Select
|
NP_000700.1:p.Ala428Asp
|
|
NM_001164783.2:c.1280C>A
|
NP_001158255.1:p.Ala427Asp
|
|