ENST00000546609.2:n.538G>T
|
|
|
ENST00000713544.1:c.707G>T
|
ENSP00000518840.1:p.Cys236Phe
|
|
ENST00000713545.1:c.684G>T
|
ENSP00000518841.1:p.Leu228=
|
|
ENST00000228606.9:c.626G>T
MANE Select
|
ENSP00000228606.4:p.Cys209Phe
|
|
ENST00000228606.8:c.626G>T
|
ENSP00000228606.4:p.Cys209Phe
|
|
ENST00000546567.5:c.-80G>T
|
ENSP00000449472.1:n.-80G>T
|
|
ENST00000546609.1:c.538G>T
|
|
|
ENST00000547344.5:n.765G>T
|
|
|
ENST00000547451.1:n.426G>T
|
|
|
NM_000785.3:c.626G>T
|
NP_000776.1:p.Cys209Phe
|
|
NM_000785.4:c.626G>T
MANE Select
|
NP_000776.1:p.Cys209Phe
|
|