ENST00000546609.2:n.693T>A
|
|
|
ENST00000713544.1:c.862T>A
|
ENSP00000518840.1:p.Phe288Ile
|
|
ENST00000713545.1:c.839T>A
|
ENSP00000518841.1:p.Val280Asp
|
|
ENST00000228606.9:c.781T>A
MANE Select
|
ENSP00000228606.4:p.Phe261Ile
|
|
ENST00000228606.8:c.781T>A
|
ENSP00000228606.4:p.Phe261Ile
|
|
ENST00000546567.5:c.76T>A
|
ENSP00000449472.1:p.Phe26Ile
|
|
ENST00000546609.1:c.693T>A
|
|
|
ENST00000547344.5:n.920T>A
|
|
|
ENST00000547451.1:n.581T>A
|
|
|
NM_000785.3:c.781T>A
|
NP_000776.1:p.Phe261Ile
|
|
NM_000785.4:c.781T>A
MANE Select
|
NP_000776.1:p.Phe261Ile
|
|