ENST00000269980.7:c.804C>G
MANE Select
|
ENSP00000269980.2:p.Gly268=
|
|
ENST00000269980.6:c.804C>G
|
ENSP00000269980.2:p.Gly268=
|
|
ENST00000457836.6:c.738C>G
|
ENSP00000416000.2:p.Gly246=
|
|
ENST00000535632.5:n.433C>G
|
|
|
ENST00000540732.3:c.906C>G
|
ENSP00000443246.1:p.Gly302=
|
|
ENST00000542943.5:c.717C>G
|
ENSP00000440345.1:p.Gly239=
|
|
ENST00000545787.1:n.432C>G
|
|
|
ENST00000595085.5:c.804C>G
|
ENSP00000471150.2:p.Gly268=
|
|
NM_000709.3:c.804C>G
|
NP_000700.1:p.Gly268=
|
|
NM_001164783.1:c.804C>G
|
NP_001158255.1:p.Gly268=
|
|
NM_000709.4:c.804C>G
MANE Select
|
NP_000700.1:p.Gly268=
|
|
NM_001164783.2:c.804C>G
|
NP_001158255.1:p.Gly268=
|
|