ENST00000682632.1:n.3981A>C
(ERCC5)
|
|
|
ENST00000682869.1:n.3529A>C
(ERCC5)
|
|
|
ENST00000683246.1:n.4517A>C
(ERCC5)
|
|
|
ENST00000683642.1:n.3110A>C
(ERCC5)
|
|
|
ENST00000639132.1:c.3555A>C
(BIVM-ERCC5)
|
ENSP00000492684.1:p.Glu1185Asp
|
|
ENST00000639435.1:c.4242A>C
(BIVM-ERCC5)
|
ENSP00000491742.1:p.Glu1414Asp
|
|
ENST00000651002.1:c.*2641A>C
(ERCC5)
|
ENSP00000498809.1:n.*2641A>C
|
|
ENST00000651055.1:n.3009-2A>C
(ERCC5)
|
|
|
ENST00000651281.1:n.3248A>C
(ERCC5)
|
|
|
ENST00000651387.1:n.2364A>C
(ERCC5)
|
|
|
ENST00000651470.1:c.*52A>C
(ERCC5)
|
ENSP00000498701.1:n.*52A>C
|
|
ENST00000652225.2:c.2880A>C
(ERCC5)
MANE Select
|
ENSP00000498881.2:p.Glu960Asp
|
|
ENST00000652613.1:c.2376A>C
(ERCC5)
|
ENSP00000498357.1:p.Glu792Asp
|
|
ENST00000355739.8:c.2880A>C
(ERCC5)
|
ENSP00000347978.4:p.Glu960Asp
|
|
ENST00000375954.1:c.579A>C
(ERCC5)
|
ENSP00000365121.1:p.Glu193Asp
|
|
ENST00000610537.4:c.2877A>C
(ERCC5)
|
ENSP00000478667.1:p.Glu959Asp
|
|
NM_000123.3:c.2880A>C , LRG_464t1:c.2880A>C
(ERCC5)
|
NP_000114.2:p.Glu960Asp
|
|
NM_001204425.1:c.4242A>C
(BIVM-ERCC5)
|
NP_001191354.1:p.Glu1414Asp
|
|
NM_000123.4:c.2880A>C
(ERCC5)
MANE Select
|
NP_000114.3:p.Glu960Asp
|
|
NM_001204425.2:c.4242A>C
(BIVM-ERCC5)
|
NP_001191354.2:p.Glu1414Asp
|
|