ENST00000559133.6:c.*170C>A
|
ENSP00000453958.2:n.*170C>A
|
|
ENST00000674301.2:c.*875C>A
|
ENSP00000501333.2:n.*875C>A
|
|
ENST00000682170.1:n.1543C>A
|
|
|
ENST00000682767.1:n.659C>A
|
|
|
ENST00000316623.10:c.7362C>A
MANE Select
|
ENSP00000325527.5:p.Pro2454=
|
|
ENST00000674301.1:c.2528C>A
|
ENSP00000501333.1:n.2528C>A
|
|
ENST00000316623.9:c.7362C>A
|
ENSP00000325527.5:p.Pro2454=
|
|
ENST00000559133.5:c.2731C>A
|
|
|
NM_000138.4:c.7362C>A , LRG_778t1:c.7362C>A
|
NP_000129.3:p.Pro2454=
|
|
NM_000138.5:c.7362C>A
MANE Select
|
NP_000129.3:p.Pro2454=
|
|