|
NM_000709.4:c.981G>T
MANE Select
|
NP_000700.1:p.Glu327Asp
|
|
ENST00000269980.7:c.981G>T
MANE Select
|
ENSP00000269980.2:p.Glu327Asp
|
|
NM_000709.3:c.981G>T
|
NP_000700.1:p.Glu327Asp
|
|
NM_001164783.1:c.978G>T
|
NP_001158255.1:p.Glu326Asp
|
|
NM_001164783.2:c.978G>T
|
NP_001158255.1:p.Glu326Asp
|
|
ENST00000269980.6:c.981G>T
|
ENSP00000269980.2:p.Glu327Asp
|
|
ENST00000457836.6:c.915G>T
|
ENSP00000416000.2:p.Glu305Asp
|
|
ENST00000535632.5:n.610G>T
|
|
|
ENST00000540732.3:c.1083G>T
|
ENSP00000443246.1:p.Glu361Asp
|
|
ENST00000542943.5:c.894G>T
|
ENSP00000440345.1:p.Glu298Asp
|
|
ENST00000595085.5:c.922+59G>T
|
ENSP00000471150.2:n.922+59G>T
|