ENST00000546609.2:n.679A>G
|
|
|
ENST00000713544.1:c.848A>G
|
ENSP00000518840.1:p.Asp283Gly
|
|
ENST00000713545.1:c.825A>G
|
ENSP00000518841.1:p.Arg275=
|
|
ENST00000228606.9:c.767A>G
MANE Select
|
ENSP00000228606.4:p.Asp256Gly
|
|
ENST00000228606.8:c.767A>G
|
ENSP00000228606.4:p.Asp256Gly
|
|
ENST00000546567.5:c.62A>G
|
ENSP00000449472.1:p.Asp21Gly
|
|
ENST00000546609.1:c.679A>G
|
|
|
ENST00000547344.5:n.906A>G
|
|
|
ENST00000547451.1:n.567A>G
|
|
|
NM_000785.3:c.767A>G
|
NP_000776.1:p.Asp256Gly
|
|
NM_000785.4:c.767A>G
MANE Select
|
NP_000776.1:p.Asp256Gly
|
|