ENST00000682632.1:n.725G>T
(ERCC5)
|
|
|
ENST00000682869.1:n.1133G>T
(ERCC5)
|
|
|
ENST00000683246.1:n.1261G>T
(ERCC5)
|
|
|
ENST00000684184.1:n.1130G>T
(ERCC5)
|
|
|
ENST00000638434.1:c.582G>T
(BIVM-ERCC5)
|
|
|
ENST00000639132.1:c.1159G>T
(BIVM-ERCC5)
|
ENSP00000492684.1:p.Glu387Ter
|
|
ENST00000639435.1:c.1846G>T
(BIVM-ERCC5)
|
ENSP00000491742.1:p.Glu616Ter
|
|
ENST00000651002.1:c.*245G>T
(ERCC5)
|
ENSP00000498809.1:n.*245G>T
|
|
ENST00000651055.1:n.613G>T
(ERCC5)
|
|
|
ENST00000651281.1:n.852G>T
(ERCC5)
|
|
|
ENST00000651470.1:c.484G>T
(ERCC5)
|
ENSP00000498701.1:p.Glu162Ter
|
|
ENST00000652225.2:c.484G>T
(ERCC5)
MANE Select
|
ENSP00000498881.2:p.Glu162Ter
|
|
ENST00000652613.1:c.-21G>T
(ERCC5)
|
ENSP00000498357.1:n.-21G>T
|
|
ENST00000355739.8:c.484G>T
(ERCC5)
|
ENSP00000347978.4:p.Glu162Ter
|
|
ENST00000535557.5:c.484G>T
(ERCC5)
|
ENSP00000442117.1:p.Glu162Ter
|
|
ENST00000602836.1:c.1760G>T
(BIVM-ERCC5)
|
|
|
ENST00000610537.4:c.484G>T
(ERCC5)
|
ENSP00000478667.1:p.Glu162Ter
|
|
NM_000123.3:c.484G>T , LRG_464t1:c.484G>T
(ERCC5)
|
NP_000114.2:p.Glu162Ter
|
|
NM_001204425.1:c.1846G>T
(BIVM-ERCC5)
|
NP_001191354.1:p.Glu616Ter
|
|
NM_000123.4:c.484G>T
(ERCC5)
MANE Select
|
NP_000114.3:p.Glu162Ter
|
|
NM_001204425.2:c.1846G>T
(BIVM-ERCC5)
|
NP_001191354.2:p.Glu616Ter
|
|