ENST00000682632.1:n.4299G=
(ERCC5)
|
|
|
ENST00000682869.1:n.3847G=
(ERCC5)
|
|
|
ENST00000683246.1:n.4835G=
(ERCC5)
|
|
|
ENST00000683642.1:n.3428G=
(ERCC5)
|
|
|
ENST00000639132.1:c.3873G=
(BIVM-ERCC5)
|
ENSP00000492684.1:p.Glu1291=
|
|
ENST00000639435.1:c.4560G=
(BIVM-ERCC5)
|
ENSP00000491742.1:p.Glu1520=
|
|
ENST00000651002.1:c.*2959G=
(ERCC5)
|
ENSP00000498809.1:n.*2959G=
|
|
ENST00000651055.1:n.3325G=
(ERCC5)
|
|
|
ENST00000651281.1:n.3566G=
(ERCC5)
|
|
|
ENST00000651387.1:n.2682G=
(ERCC5)
|
|
|
ENST00000651470.1:c.*370G=
(ERCC5)
|
ENSP00000498701.1:n.*370G=
|
|
ENST00000652225.2:c.3198G=
(ERCC5)
MANE Select
|
ENSP00000498881.2:p.Glu1066=
|
|
ENST00000652613.1:c.2694G=
(ERCC5)
|
ENSP00000498357.1:p.Glu898=
|
|
ENST00000355739.8:c.3198G=
(ERCC5)
|
ENSP00000347978.4:p.Glu1066=
|
|
ENST00000375954.1:c.897G=
(ERCC5)
|
ENSP00000365121.1:p.Glu299=
|
|
ENST00000472247.1:n.358G=
(ERCC5)
|
|
|
ENST00000610537.4:c.3195G=
(ERCC5)
|
ENSP00000478667.1:p.Glu1065=
|
|
NM_000123.3:c.3198G= , LRG_464t1:c.3198G=
(ERCC5)
|
NP_000114.2:p.Glu1066=
|
|
NM_001204425.1:c.4560G=
(BIVM-ERCC5)
|
NP_001191354.1:p.Glu1520=
|
|
NM_000123.4:c.3198G=
(ERCC5)
MANE Select
|
NP_000114.3:p.Glu1066=
|
|
NM_001204425.2:c.4560G=
(BIVM-ERCC5)
|
NP_001191354.2:p.Glu1520=
|
|