ENST00000546609.2:n.595T>G
|
|
|
ENST00000713544.1:c.764T>G
|
ENSP00000518840.1:p.Val255Gly
|
|
ENST00000713545.1:c.741T>G
|
ENSP00000518841.1:p.Gly247=
|
|
ENST00000228606.9:c.683T>G
MANE Select
|
ENSP00000228606.4:p.Val228Gly
|
|
ENST00000228606.8:c.683T>G
|
ENSP00000228606.4:p.Val228Gly
|
|
ENST00000546567.5:c.-23T>G
|
ENSP00000449472.1:n.-23T>G
|
|
ENST00000546609.1:c.595T>G
|
|
|
ENST00000547344.5:n.822T>G
|
|
|
ENST00000547451.1:n.483T>G
|
|
|
NM_000785.3:c.683T>G
|
NP_000776.1:p.Val228Gly
|
|
NM_000785.4:c.683T>G
MANE Select
|
NP_000776.1:p.Val228Gly
|
|