ENST00000269980.7:c.413A>G
MANE Select
|
ENSP00000269980.2:p.Glu138Gly
|
|
ENST00000269980.6:c.413A>G
|
ENSP00000269980.2:p.Glu138Gly
|
|
ENST00000457836.6:c.347A>G
|
ENSP00000416000.2:p.Glu116Gly
|
|
ENST00000538423.5:n.539A>G
|
|
|
ENST00000540732.3:c.515A>G
|
ENSP00000443246.1:p.Glu172Gly
|
|
ENST00000541315.1:c.220A>G
|
|
|
ENST00000542943.5:c.326A>G
|
ENSP00000440345.1:p.Glu109Gly
|
|
ENST00000595085.5:c.413A>G
|
ENSP00000471150.2:p.Glu138Gly
|
|
NM_000709.3:c.413A>G
|
NP_000700.1:p.Glu138Gly
|
|
NM_001164783.1:c.413A>G
|
NP_001158255.1:p.Glu138Gly
|
|
NM_000709.4:c.413A>G
MANE Select
|
NP_000700.1:p.Glu138Gly
|
|
NM_001164783.2:c.413A>G
|
NP_001158255.1:p.Glu138Gly
|
|