ENST00000269980.7:c.1309C>G
MANE Select
|
ENSP00000269980.2:p.His437Asp
|
|
ENST00000269980.6:c.1309C>G
|
ENSP00000269980.2:p.His437Asp
|
|
ENST00000457836.6:c.1318C>G
|
ENSP00000416000.2:p.His440Asp
|
|
ENST00000540732.3:c.1411C>G
|
ENSP00000443246.1:p.His471Asp
|
|
ENST00000544905.1:c.139C>G
|
|
|
ENST00000595085.5:c.922+1882C>G
|
ENSP00000471150.2:n.922+1882C>G
|
|
NM_000709.3:c.1309C>G
|
NP_000700.1:p.His437Asp
|
|
NM_001164783.1:c.1306C>G
|
NP_001158255.1:p.His436Asp
|
|
NM_000709.4:c.1309C>G
MANE Select
|
NP_000700.1:p.His437Asp
|
|
NM_001164783.2:c.1306C>G
|
NP_001158255.1:p.His436Asp
|
|