ENST00000546609.2:n.598T>A
|
|
|
ENST00000713544.1:c.767T>A
|
ENSP00000518840.1:p.Phe256Tyr
|
|
ENST00000713545.1:c.744T>A
|
ENSP00000518841.1:p.Val248=
|
|
ENST00000228606.9:c.686T>A
MANE Select
|
ENSP00000228606.4:p.Phe229Tyr
|
|
ENST00000228606.8:c.686T>A
|
ENSP00000228606.4:p.Phe229Tyr
|
|
ENST00000546567.5:c.-20T>A
|
ENSP00000449472.1:n.-20T>A
|
|
ENST00000546609.1:c.598T>A
|
|
|
ENST00000547344.5:n.825T>A
|
|
|
ENST00000547451.1:n.486T>A
|
|
|
NM_000785.3:c.686T>A
|
NP_000776.1:p.Phe229Tyr
|
|
NM_000785.4:c.686T>A
MANE Select
|
NP_000776.1:p.Phe229Tyr
|
|