ENST00000682632.1:n.4398A>C
(ERCC5)
|
|
|
ENST00000682869.1:n.3946A>C
(ERCC5)
|
|
|
ENST00000683246.1:n.4934A>C
(ERCC5)
|
|
|
ENST00000683642.1:n.3527A>C
(ERCC5)
|
|
|
ENST00000639132.1:c.3972A>C
(BIVM-ERCC5)
|
ENSP00000492684.1:p.Gly1324=
|
|
ENST00000639435.1:c.4659A>C
(BIVM-ERCC5)
|
ENSP00000491742.1:p.Gly1553=
|
|
ENST00000651002.1:c.*3058A>C
(ERCC5)
|
ENSP00000498809.1:n.*3058A>C
|
|
ENST00000651055.1:n.3424A>C
(ERCC5)
|
|
|
ENST00000651281.1:n.3665A>C
(ERCC5)
|
|
|
ENST00000651387.1:n.2781A>C
(ERCC5)
|
|
|
ENST00000651470.1:c.*469A>C
(ERCC5)
|
ENSP00000498701.1:n.*469A>C
|
|
ENST00000652225.2:c.3297A>C
(ERCC5)
MANE Select
|
ENSP00000498881.2:p.Gly1099=
|
|
ENST00000652613.1:c.2793A>C
(ERCC5)
|
ENSP00000498357.1:p.Gly931=
|
|
ENST00000355739.8:c.3297A>C
(ERCC5)
|
ENSP00000347978.4:p.Gly1099=
|
|
ENST00000375954.1:c.996A>C
(ERCC5)
|
ENSP00000365121.1:p.Gly332=
|
|
ENST00000472247.1:n.457A>C
(ERCC5)
|
|
|
ENST00000610537.4:c.3294A>C
(ERCC5)
|
ENSP00000478667.1:p.Gly1098=
|
|
NM_000123.3:c.3297A>C , LRG_464t1:c.3297A>C
(ERCC5)
|
NP_000114.2:p.Gly1099=
|
|
NM_001204425.1:c.4659A>C
(BIVM-ERCC5)
|
NP_001191354.1:p.Gly1553=
|
|
NM_000123.4:c.3297A>C
(ERCC5)
MANE Select
|
NP_000114.3:p.Gly1099=
|
|
NM_001204425.2:c.4659A>C
(BIVM-ERCC5)
|
NP_001191354.2:p.Gly1553=
|
|