ENST00000546609.2:n.568A>T
|
|
|
ENST00000713544.1:c.737A>T
|
ENSP00000518840.1:p.Glu246Val
|
|
ENST00000713545.1:c.714A>T
|
ENSP00000518841.1:p.Gly238=
|
|
ENST00000228606.9:c.656A>T
MANE Select
|
ENSP00000228606.4:p.Glu219Val
|
|
ENST00000228606.8:c.656A>T
|
ENSP00000228606.4:p.Glu219Val
|
|
ENST00000546567.5:c.-50A>T
|
ENSP00000449472.1:n.-50A>T
|
|
ENST00000546609.1:c.568A>T
|
|
|
ENST00000547344.5:n.795A>T
|
|
|
ENST00000547451.1:n.456A>T
|
|
|
NM_000785.3:c.656A>T
|
NP_000776.1:p.Glu219Val
|
|
NM_000785.4:c.656A>T
MANE Select
|
NP_000776.1:p.Glu219Val
|
|