ENST00000559133.6:c.6876G>T
|
ENSP00000453958.2:p.Glu2292Asp
|
|
ENST00000674301.2:c.*327G>T
|
ENSP00000501333.2:n.*327G>T
|
|
ENST00000682170.1:n.485G>T
|
|
|
ENST00000682767.1:n.111G>T
|
|
|
ENST00000316623.10:c.6876G>T
MANE Select
|
ENSP00000325527.5:p.Glu2292Asp
|
|
ENST00000674301.1:c.1980G>T
|
ENSP00000501333.1:n.1980G>T
|
|
ENST00000316623.9:c.6876G>T
|
ENSP00000325527.5:p.Glu2292Asp
|
|
ENST00000559133.5:c.2183G>T
|
|
|
ENST00000560720.1:n.163G>T
|
|
|
NM_000138.4:c.6876G>T , LRG_778t1:c.6876G>T
|
NP_000129.3:p.Glu2292Asp
|
|
NM_000138.5:c.6876G>T
MANE Select
|
NP_000129.3:p.Glu2292Asp
|
|