ENST00000546609.2:n.597T>A
|
|
|
ENST00000713544.1:c.766T>A
|
ENSP00000518840.1:p.Phe256Ile
|
|
ENST00000713545.1:c.743T>A
|
ENSP00000518841.1:p.Val248Asp
|
|
ENST00000228606.9:c.685T>A
MANE Select
|
ENSP00000228606.4:p.Phe229Ile
|
|
ENST00000228606.8:c.685T>A
|
ENSP00000228606.4:p.Phe229Ile
|
|
ENST00000546567.5:c.-21T>A
|
ENSP00000449472.1:n.-21T>A
|
|
ENST00000546609.1:c.597T>A
|
|
|
ENST00000547344.5:n.824T>A
|
|
|
ENST00000547451.1:n.485T>A
|
|
|
NM_000785.3:c.685T>A
|
NP_000776.1:p.Phe229Ile
|
|
NM_000785.4:c.685T>A
MANE Select
|
NP_000776.1:p.Phe229Ile
|
|