ENST00000546609.2:n.701T>G
|
|
|
ENST00000713544.1:c.870T>G
|
ENSP00000518840.1:p.Phe290Leu
|
|
ENST00000713545.1:c.847T>G
|
ENSP00000518841.1:p.Cys283Gly
|
|
ENST00000228606.9:c.789T>G
MANE Select
|
ENSP00000228606.4:p.Phe263Leu
|
|
ENST00000228606.8:c.789T>G
|
ENSP00000228606.4:p.Phe263Leu
|
|
ENST00000546567.5:c.84T>G
|
ENSP00000449472.1:p.Phe28Leu
|
|
ENST00000546609.1:c.701T>G
|
|
|
ENST00000547344.5:n.928T>G
|
|
|
ENST00000547451.1:n.589T>G
|
|
|
NM_000785.3:c.789T>G
|
NP_000776.1:p.Phe263Leu
|
|
NM_000785.4:c.789T>G
MANE Select
|
NP_000776.1:p.Phe263Leu
|
|