ENST00000559133.6:c.*241A>T
|
ENSP00000453958.2:n.*241A>T
|
|
ENST00000674301.2:c.*946A>T
|
ENSP00000501333.2:n.*946A>T
|
|
ENST00000682170.1:n.1614A>T
|
|
|
ENST00000682767.1:n.730A>T
|
|
|
ENST00000316623.10:c.7433A>T
MANE Select
|
ENSP00000325527.5:p.Glu2478Val
|
|
ENST00000674301.1:c.2599A>T
|
ENSP00000501333.1:n.2599A>T
|
|
ENST00000316623.9:c.7433A>T
|
ENSP00000325527.5:p.Glu2478Val
|
|
ENST00000559133.5:c.2802A>T
|
|
|
NM_000138.4:c.7433A>T , LRG_778t1:c.7433A>T
|
NP_000129.3:p.Glu2478Val
|
|
NM_000138.5:c.7433A>T
MANE Select
|
NP_000129.3:p.Glu2478Val
|
|