ENST00000546609.2:n.537T>A
|
|
|
ENST00000713544.1:c.706T>A
|
ENSP00000518840.1:p.Cys236Ser
|
|
ENST00000713545.1:c.683T>A
|
ENSP00000518841.1:p.Leu228Gln
|
|
ENST00000228606.9:c.625T>A
MANE Select
|
ENSP00000228606.4:p.Cys209Ser
|
|
ENST00000228606.8:c.625T>A
|
ENSP00000228606.4:p.Cys209Ser
|
|
ENST00000546567.5:c.-81T>A
|
ENSP00000449472.1:n.-81T>A
|
|
ENST00000546609.1:c.537T>A
|
|
|
ENST00000547344.5:n.764T>A
|
|
|
ENST00000547451.1:n.425T>A
|
|
|
NM_000785.3:c.625T>A
|
NP_000776.1:p.Cys209Ser
|
|
NM_000785.4:c.625T>A
MANE Select
|
NP_000776.1:p.Cys209Ser
|
|