ENST00000682632.1:n.4326T>C
(ERCC5)
|
|
|
ENST00000682869.1:n.3874T>C
(ERCC5)
|
|
|
ENST00000683246.1:n.4862T>C
(ERCC5)
|
|
|
ENST00000683642.1:n.3455T>C
(ERCC5)
|
|
|
ENST00000639132.1:c.3900T>C
(BIVM-ERCC5)
|
ENSP00000492684.1:p.Leu1300=
|
|
ENST00000639435.1:c.4587T>C
(BIVM-ERCC5)
|
ENSP00000491742.1:p.Leu1529=
|
|
ENST00000651002.1:c.*2986T>C
(ERCC5)
|
ENSP00000498809.1:n.*2986T>C
|
|
ENST00000651055.1:n.3352T>C
(ERCC5)
|
|
|
ENST00000651281.1:n.3593T>C
(ERCC5)
|
|
|
ENST00000651387.1:n.2709T>C
(ERCC5)
|
|
|
ENST00000651470.1:c.*397T>C
(ERCC5)
|
ENSP00000498701.1:n.*397T>C
|
|
ENST00000652225.2:c.3225T>C
(ERCC5)
MANE Select
|
ENSP00000498881.2:p.Leu1075=
|
|
ENST00000652613.1:c.2721T>C
(ERCC5)
|
ENSP00000498357.1:p.Leu907=
|
|
ENST00000355739.8:c.3225T>C
(ERCC5)
|
ENSP00000347978.4:p.Leu1075=
|
|
ENST00000375954.1:c.924T>C
(ERCC5)
|
ENSP00000365121.1:p.Leu308=
|
|
ENST00000472247.1:n.385T>C
(ERCC5)
|
|
|
ENST00000610537.4:c.3222T>C
(ERCC5)
|
ENSP00000478667.1:p.Leu1074=
|
|
NM_000123.3:c.3225T>C , LRG_464t1:c.3225T>C
(ERCC5)
|
NP_000114.2:p.Leu1075=
|
|
NM_001204425.1:c.4587T>C
(BIVM-ERCC5)
|
NP_001191354.1:p.Leu1529=
|
|
NM_000123.4:c.3225T>C
(ERCC5)
MANE Select
|
NP_000114.3:p.Leu1075=
|
|
NM_001204425.2:c.4587T>C
(BIVM-ERCC5)
|
NP_001191354.2:p.Leu1529=
|
|