ENST00000682632.1:n.4406G>C
(ERCC5)
|
|
|
ENST00000682869.1:n.3954G>C
(ERCC5)
|
|
|
ENST00000683246.1:n.4942G>C
(ERCC5)
|
|
|
ENST00000683642.1:n.3535G>C
(ERCC5)
|
|
|
ENST00000639132.1:c.3980G>C
(BIVM-ERCC5)
|
ENSP00000492684.1:p.Ser1327Thr
|
|
ENST00000639435.1:c.4667G>C
(BIVM-ERCC5)
|
ENSP00000491742.1:p.Ser1556Thr
|
|
ENST00000651002.1:c.*3066G>C
(ERCC5)
|
ENSP00000498809.1:n.*3066G>C
|
|
ENST00000651055.1:n.3432G>C
(ERCC5)
|
|
|
ENST00000651281.1:n.3673G>C
(ERCC5)
|
|
|
ENST00000651387.1:n.2789G>C
(ERCC5)
|
|
|
ENST00000651470.1:c.*477G>C
(ERCC5)
|
ENSP00000498701.1:n.*477G>C
|
|
ENST00000652225.2:c.3305G>C
(ERCC5)
MANE Select
|
ENSP00000498881.2:p.Ser1102Thr
|
|
ENST00000652613.1:c.2801G>C
(ERCC5)
|
ENSP00000498357.1:p.Ser934Thr
|
|
ENST00000355739.8:c.3305G>C
(ERCC5)
|
ENSP00000347978.4:p.Ser1102Thr
|
|
ENST00000375954.1:c.1004G>C
(ERCC5)
|
ENSP00000365121.1:p.Ser335Thr
|
|
ENST00000472247.1:n.465G>C
(ERCC5)
|
|
|
ENST00000610537.4:c.3302G>C
(ERCC5)
|
ENSP00000478667.1:p.Ser1101Thr
|
|
NM_000123.3:c.3305G>C , LRG_464t1:c.3305G>C
(ERCC5)
|
NP_000114.2:p.Ser1102Thr
|
|
NM_001204425.1:c.4667G>C
(BIVM-ERCC5)
|
NP_001191354.1:p.Ser1556Thr
|
|
NM_000123.4:c.3305G>C
(ERCC5)
MANE Select
|
NP_000114.3:p.Ser1102Thr
|
|
NM_001204425.2:c.4667G>C
(BIVM-ERCC5)
|
NP_001191354.2:p.Ser1556Thr
|
|