ENST00000682632.1:n.4371G>A
(ERCC5)
|
|
|
ENST00000682869.1:n.3919G>A
(ERCC5)
|
|
|
ENST00000683246.1:n.4907G>A
(ERCC5)
|
|
|
ENST00000683642.1:n.3500G>A
(ERCC5)
|
|
|
ENST00000639132.1:c.3945G>A
(BIVM-ERCC5)
|
ENSP00000492684.1:p.Glu1315=
|
|
ENST00000639435.1:c.4632G>A
(BIVM-ERCC5)
|
ENSP00000491742.1:p.Glu1544=
|
|
ENST00000651002.1:c.*3031G>A
(ERCC5)
|
ENSP00000498809.1:n.*3031G>A
|
|
ENST00000651055.1:n.3397G>A
(ERCC5)
|
|
|
ENST00000651281.1:n.3638G>A
(ERCC5)
|
|
|
ENST00000651387.1:n.2754G>A
(ERCC5)
|
|
|
ENST00000651470.1:c.*442G>A
(ERCC5)
|
ENSP00000498701.1:n.*442G>A
|
|
ENST00000652225.2:c.3270G>A
(ERCC5)
MANE Select
|
ENSP00000498881.2:p.Glu1090=
|
|
ENST00000652613.1:c.2766G>A
(ERCC5)
|
ENSP00000498357.1:p.Glu922=
|
|
ENST00000355739.8:c.3270G>A
(ERCC5)
|
ENSP00000347978.4:p.Glu1090=
|
|
ENST00000375954.1:c.969G>A
(ERCC5)
|
ENSP00000365121.1:p.Glu323=
|
|
ENST00000472247.1:n.430G>A
(ERCC5)
|
|
|
ENST00000610537.4:c.3267G>A
(ERCC5)
|
ENSP00000478667.1:p.Glu1089=
|
|
NM_000123.3:c.3270G>A , LRG_464t1:c.3270G>A
(ERCC5)
|
NP_000114.2:p.Glu1090=
|
|
NM_001204425.1:c.4632G>A
(BIVM-ERCC5)
|
NP_001191354.1:p.Glu1544=
|
|
NM_000123.4:c.3270G>A
(ERCC5)
MANE Select
|
NP_000114.3:p.Glu1090=
|
|
NM_001204425.2:c.4632G>A
(BIVM-ERCC5)
|
NP_001191354.2:p.Glu1544=
|
|