ENST00000682632.1:n.4409A>T
(ERCC5)
|
|
|
ENST00000682869.1:n.3957A>T
(ERCC5)
|
|
|
ENST00000683246.1:n.4945A>T
(ERCC5)
|
|
|
ENST00000683642.1:n.3538A>T
(ERCC5)
|
|
|
ENST00000639132.1:c.3983A>T
(BIVM-ERCC5)
|
ENSP00000492684.1:p.Glu1328Val
|
|
ENST00000639435.1:c.4670A>T
(BIVM-ERCC5)
|
ENSP00000491742.1:p.Glu1557Val
|
|
ENST00000651002.1:c.*3069A>T
(ERCC5)
|
ENSP00000498809.1:n.*3069A>T
|
|
ENST00000651055.1:n.3435A>T
(ERCC5)
|
|
|
ENST00000651281.1:n.3676A>T
(ERCC5)
|
|
|
ENST00000651387.1:n.2792A>T
(ERCC5)
|
|
|
ENST00000651470.1:c.*480A>T
(ERCC5)
|
ENSP00000498701.1:n.*480A>T
|
|
ENST00000652225.2:c.3308A>T
(ERCC5)
MANE Select
|
ENSP00000498881.2:p.Glu1103Val
|
|
ENST00000652613.1:c.2804A>T
(ERCC5)
|
ENSP00000498357.1:p.Glu935Val
|
|
ENST00000355739.8:c.3308A>T
(ERCC5)
|
ENSP00000347978.4:p.Glu1103Val
|
|
ENST00000375954.1:c.1007A>T
(ERCC5)
|
ENSP00000365121.1:p.Glu336Val
|
|
ENST00000472247.1:n.468A>T
(ERCC5)
|
|
|
ENST00000610537.4:c.3305A>T
(ERCC5)
|
ENSP00000478667.1:p.Glu1102Val
|
|
NM_000123.3:c.3308A>T , LRG_464t1:c.3308A>T
(ERCC5)
|
NP_000114.2:p.Glu1103Val
|
|
NM_001204425.1:c.4670A>T
(BIVM-ERCC5)
|
NP_001191354.1:p.Glu1557Val
|
|
NM_000123.4:c.3308A>T
(ERCC5)
MANE Select
|
NP_000114.3:p.Glu1103Val
|
|
NM_001204425.2:c.4670A>T
(BIVM-ERCC5)
|
NP_001191354.2:p.Glu1557Val
|
|