ENST00000269980.7:c.1321G>C
MANE Select
|
ENSP00000269980.2:p.Asp441His
|
|
ENST00000269980.6:c.1321G>C
|
ENSP00000269980.2:p.Asp441His
|
|
ENST00000457836.6:c.1330G>C
|
ENSP00000416000.2:p.Asp444His
|
|
ENST00000540732.3:c.1423G>C
|
ENSP00000443246.1:p.Asp475His
|
|
ENST00000544905.1:c.151G>C
|
|
|
ENST00000595085.5:c.922+1894G>C
|
ENSP00000471150.2:n.922+1894G>C
|
|
NM_000709.3:c.1321G>C
|
NP_000700.1:p.Asp441His
|
|
NM_001164783.1:c.1318G>C
|
NP_001158255.1:p.Asp440His
|
|
NM_000709.4:c.1321G>C
MANE Select
|
NP_000700.1:p.Asp441His
|
|
NM_001164783.2:c.1318G>C
|
NP_001158255.1:p.Asp440His
|
|