|
NM_000138.5:c.7850G>A
MANE Select
|
NP_000129.3:p.Cys2617Tyr
|
|
ENST00000316623.10:c.7850G>A
MANE Select
|
ENSP00000325527.5:p.Cys2617Tyr
|
|
NM_000138.4:c.7850G>A , LRG_778t1:c.7850G>A
|
NP_000129.3:p.Cys2617Tyr
|
|
ENST00000316623.9:c.7850G>A
|
ENSP00000325527.5:p.Cys2617Tyr
|
|
ENST00000559133.5:c.3219G>A
|
|
|
ENST00000559133.6:c.*658G>A
|
ENSP00000453958.2:n.*658G>A
|
|
ENST00000561429.1:n.105G>A
|
|
|
ENST00000674301.1:c.3016G>A
|
ENSP00000501333.1:n.3016G>A
|
|
ENST00000674301.2:c.*1363G>A
|
ENSP00000501333.2:n.*1363G>A
|
|
ENST00000682158.1:n.1231G>A
|
|
|
ENST00000682170.1:n.2031G>A
|
|
|
ENST00000682767.1:n.1147G>A
|
|