ENST00000559133.6:c.*984C>A
|
ENSP00000453958.2:n.*984C>A
|
|
ENST00000674301.2:c.*1689C>A
|
ENSP00000501333.2:n.*1689C>A
|
|
ENST00000682158.1:n.1557C>A
|
|
|
ENST00000682170.1:n.2357C>A
|
|
|
ENST00000682767.1:n.1473C>A
|
|
|
ENST00000316623.10:c.8176C>A
MANE Select
|
ENSP00000325527.5:p.Arg2726=
|
|
ENST00000674301.1:c.3342C>A
|
ENSP00000501333.1:n.3342C>A
|
|
ENST00000316623.9:c.8176C>A
|
ENSP00000325527.5:p.Arg2726=
|
|
ENST00000559133.5:c.3545C>A
|
|
|
ENST00000561429.1:n.431C>A
|
|
|
NM_000138.4:c.8176C>A , LRG_778t1:c.8176C>A
|
NP_000129.3:p.Arg2726=
|
|
NM_000138.5:c.8176C>A
MANE Select
|
NP_000129.3:p.Arg2726=
|
|