ENST00000682632.1:n.4396G>T
(ERCC5)
|
|
|
ENST00000682869.1:n.3944G>T
(ERCC5)
|
|
|
ENST00000683246.1:n.4932G>T
(ERCC5)
|
|
|
ENST00000683642.1:n.3525G>T
(ERCC5)
|
|
|
ENST00000639132.1:c.3970G>T
(BIVM-ERCC5)
|
ENSP00000492684.1:p.Gly1324Ter
|
|
ENST00000639435.1:c.4657G>T
(BIVM-ERCC5)
|
ENSP00000491742.1:p.Gly1553Ter
|
|
ENST00000651002.1:c.*3056G>T
(ERCC5)
|
ENSP00000498809.1:n.*3056G>T
|
|
ENST00000651055.1:n.3422G>T
(ERCC5)
|
|
|
ENST00000651281.1:n.3663G>T
(ERCC5)
|
|
|
ENST00000651387.1:n.2779G>T
(ERCC5)
|
|
|
ENST00000651470.1:c.*467G>T
(ERCC5)
|
ENSP00000498701.1:n.*467G>T
|
|
ENST00000652225.2:c.3295G>T
(ERCC5)
MANE Select
|
ENSP00000498881.2:p.Gly1099Ter
|
|
ENST00000652613.1:c.2791G>T
(ERCC5)
|
ENSP00000498357.1:p.Gly931Ter
|
|
ENST00000355739.8:c.3295G>T
(ERCC5)
|
ENSP00000347978.4:p.Gly1099Ter
|
|
ENST00000375954.1:c.994G>T
(ERCC5)
|
ENSP00000365121.1:p.Gly332Ter
|
|
ENST00000472247.1:n.455G>T
(ERCC5)
|
|
|
ENST00000610537.4:c.3292G>T
(ERCC5)
|
ENSP00000478667.1:p.Gly1098Ter
|
|
NM_000123.3:c.3295G>T , LRG_464t1:c.3295G>T
(ERCC5)
|
NP_000114.2:p.Gly1099Ter
|
|
NM_001204425.1:c.4657G>T
(BIVM-ERCC5)
|
NP_001191354.1:p.Gly1553Ter
|
|
NM_000123.4:c.3295G>T
(ERCC5)
MANE Select
|
NP_000114.3:p.Gly1099Ter
|
|
NM_001204425.2:c.4657G>T
(BIVM-ERCC5)
|
NP_001191354.2:p.Gly1553Ter
|
|