ENST00000682632.1:n.4367G>T
(ERCC5)
|
|
|
ENST00000682869.1:n.3915G>T
(ERCC5)
|
|
|
ENST00000683246.1:n.4903G>T
(ERCC5)
|
|
|
ENST00000683642.1:n.3496G>T
(ERCC5)
|
|
|
ENST00000639132.1:c.3941G>T
(BIVM-ERCC5)
|
ENSP00000492684.1:p.Gly1314Val
|
|
ENST00000639435.1:c.4628G>T
(BIVM-ERCC5)
|
ENSP00000491742.1:p.Gly1543Val
|
|
ENST00000651002.1:c.*3027G>T
(ERCC5)
|
ENSP00000498809.1:n.*3027G>T
|
|
ENST00000651055.1:n.3393G>T
(ERCC5)
|
|
|
ENST00000651281.1:n.3634G>T
(ERCC5)
|
|
|
ENST00000651387.1:n.2750G>T
(ERCC5)
|
|
|
ENST00000651470.1:c.*438G>T
(ERCC5)
|
ENSP00000498701.1:n.*438G>T
|
|
ENST00000652225.2:c.3266G>T
(ERCC5)
MANE Select
|
ENSP00000498881.2:p.Gly1089Val
|
|
ENST00000652613.1:c.2762G>T
(ERCC5)
|
ENSP00000498357.1:p.Gly921Val
|
|
ENST00000355739.8:c.3266G>T
(ERCC5)
|
ENSP00000347978.4:p.Gly1089Val
|
|
ENST00000375954.1:c.965G>T
(ERCC5)
|
ENSP00000365121.1:p.Gly322Val
|
|
ENST00000472247.1:n.426G>T
(ERCC5)
|
|
|
ENST00000610537.4:c.3263G>T
(ERCC5)
|
ENSP00000478667.1:p.Gly1088Val
|
|
NM_000123.3:c.3266G>T , LRG_464t1:c.3266G>T
(ERCC5)
|
NP_000114.2:p.Gly1089Val
|
|
NM_001204425.1:c.4628G>T
(BIVM-ERCC5)
|
NP_001191354.1:p.Gly1543Val
|
|
NM_000123.4:c.3266G>T
(ERCC5)
MANE Select
|
NP_000114.3:p.Gly1089Val
|
|
NM_001204425.2:c.4628G>T
(BIVM-ERCC5)
|
NP_001191354.2:p.Gly1543Val
|
|