ENST00000546609.2:n.601T>C
|
|
|
ENST00000713544.1:c.770T>C
|
ENSP00000518840.1:p.Val257Ala
|
|
ENST00000713545.1:c.747T>C
|
ENSP00000518841.1:p.Cys249=
|
|
ENST00000228606.9:c.689T>C
MANE Select
|
ENSP00000228606.4:p.Val230Ala
|
|
ENST00000228606.8:c.689T>C
|
ENSP00000228606.4:p.Val230Ala
|
|
ENST00000546567.5:c.-17T>C
|
ENSP00000449472.1:n.-17T>C
|
|
ENST00000546609.1:c.601T>C
|
|
|
ENST00000547344.5:n.828T>C
|
|
|
ENST00000547451.1:n.489T>C
|
|
|
NM_000785.3:c.689T>C
|
NP_000776.1:p.Val230Ala
|
|
NM_000785.4:c.689T>C
MANE Select
|
NP_000776.1:p.Val230Ala
|
|