ENST00000559133.6:c.*478C>A
|
ENSP00000453958.2:n.*478C>A
|
|
ENST00000674301.2:c.*1183C>A
|
ENSP00000501333.2:n.*1183C>A
|
|
ENST00000682170.1:n.1851C>A
|
|
|
ENST00000682767.1:n.967C>A
|
|
|
ENST00000316623.10:c.7670C>A
MANE Select
|
ENSP00000325527.5:p.Ser2557Ter
|
|
ENST00000674301.1:c.2836C>A
|
ENSP00000501333.1:n.2836C>A
|
|
ENST00000316623.9:c.7670C>A
|
ENSP00000325527.5:p.Ser2557Ter
|
|
ENST00000559133.5:c.3039C>A
|
|
|
NM_000138.4:c.7670C>A , LRG_778t1:c.7670C>A
|
NP_000129.3:p.Ser2557Ter
|
|
NM_000138.5:c.7670C>A
MANE Select
|
NP_000129.3:p.Ser2557Ter
|
|