ENST00000546609.2:n.537T>G
|
|
|
ENST00000713544.1:c.706T>G
|
ENSP00000518840.1:p.Cys236Gly
|
|
ENST00000713545.1:c.683T>G
|
ENSP00000518841.1:p.Leu228Arg
|
|
ENST00000228606.9:c.625T>G
MANE Select
|
ENSP00000228606.4:p.Cys209Gly
|
|
ENST00000228606.8:c.625T>G
|
ENSP00000228606.4:p.Cys209Gly
|
|
ENST00000546567.5:c.-81T>G
|
ENSP00000449472.1:n.-81T>G
|
|
ENST00000546609.1:c.537T>G
|
|
|
ENST00000547344.5:n.764T>G
|
|
|
ENST00000547451.1:n.425T>G
|
|
|
NM_000785.3:c.625T>G
|
NP_000776.1:p.Cys209Gly
|
|
NM_000785.4:c.625T>G
MANE Select
|
NP_000776.1:p.Cys209Gly
|
|