ENST00000559133.6:c.*1216T>A
|
ENSP00000453958.2:n.*1216T>A
|
|
ENST00000674301.2:c.*1921T>A
|
ENSP00000501333.2:n.*1921T>A
|
|
ENST00000682158.1:n.1789T>A
|
|
|
ENST00000682170.1:n.2589T>A
|
|
|
ENST00000682767.1:n.1705T>A
|
|
|
ENST00000316623.10:c.8408T>A
MANE Select
|
ENSP00000325527.5:p.Phe2803Tyr
|
|
ENST00000674301.1:c.3574T>A
|
ENSP00000501333.1:n.3574T>A
|
|
ENST00000316623.9:c.8408T>A
|
ENSP00000325527.5:p.Phe2803Tyr
|
|
ENST00000559133.5:c.3777T>A
|
|
|
NM_000138.4:c.8408T>A , LRG_778t1:c.8408T>A
|
NP_000129.3:p.Phe2803Tyr
|
|
NM_000138.5:c.8408T>A
MANE Select
|
NP_000129.3:p.Phe2803Tyr
|
|