ENST00000546609.2:n.539C>G
|
|
|
ENST00000713544.1:c.708C>G
|
ENSP00000518840.1:p.Cys236Trp
|
|
ENST00000713545.1:c.685C>G
|
ENSP00000518841.1:p.Pro229Ala
|
|
ENST00000228606.9:c.627C>G
MANE Select
|
ENSP00000228606.4:p.Cys209Trp
|
|
ENST00000228606.8:c.627C>G
|
ENSP00000228606.4:p.Cys209Trp
|
|
ENST00000546567.5:c.-79C>G
|
ENSP00000449472.1:n.-79C>G
|
|
ENST00000546609.1:c.539C>G
|
|
|
ENST00000547344.5:n.766C>G
|
|
|
ENST00000547451.1:n.427C>G
|
|
|
NM_000785.3:c.627C>G
|
NP_000776.1:p.Cys209Trp
|
|
NM_000785.4:c.627C>G
MANE Select
|
NP_000776.1:p.Cys209Trp
|
|