ENST00000682632.1:n.4040T>G
(ERCC5)
|
|
|
ENST00000682869.1:n.3588T>G
(ERCC5)
|
|
|
ENST00000683246.1:n.4576T>G
(ERCC5)
|
|
|
ENST00000683642.1:n.3169T>G
(ERCC5)
|
|
|
ENST00000639132.1:c.3614T>G
(BIVM-ERCC5)
|
ENSP00000492684.1:p.Val1205Gly
|
|
ENST00000639435.1:c.4301T>G
(BIVM-ERCC5)
|
ENSP00000491742.1:p.Val1434Gly
|
|
ENST00000651002.1:c.*2700T>G
(ERCC5)
|
ENSP00000498809.1:n.*2700T>G
|
|
ENST00000651055.1:n.3066T>G
(ERCC5)
|
|
|
ENST00000651281.1:n.3307T>G
(ERCC5)
|
|
|
ENST00000651387.1:n.2423T>G
(ERCC5)
|
|
|
ENST00000651470.1:c.*111T>G
(ERCC5)
|
ENSP00000498701.1:n.*111T>G
|
|
ENST00000652225.2:c.2939T>G
(ERCC5)
MANE Select
|
ENSP00000498881.2:p.Val980Gly
|
|
ENST00000652613.1:c.2435T>G
(ERCC5)
|
ENSP00000498357.1:p.Val812Gly
|
|
ENST00000355739.8:c.2939T>G
(ERCC5)
|
ENSP00000347978.4:p.Val980Gly
|
|
ENST00000375954.1:c.638T>G
(ERCC5)
|
ENSP00000365121.1:p.Val213Gly
|
|
ENST00000610537.4:c.2936T>G
(ERCC5)
|
ENSP00000478667.1:p.Val979Gly
|
|
NM_000123.3:c.2939T>G , LRG_464t1:c.2939T>G
(ERCC5)
|
NP_000114.2:p.Val980Gly
|
|
NM_001204425.1:c.4301T>G
(BIVM-ERCC5)
|
NP_001191354.1:p.Val1434Gly
|
|
NM_000123.4:c.2939T>G
(ERCC5)
MANE Select
|
NP_000114.3:p.Val980Gly
|
|
NM_001204425.2:c.4301T>G
(BIVM-ERCC5)
|
NP_001191354.2:p.Val1434Gly
|
|