|
ENST00000682632.1:n.1999A>T
(ERCC5)
|
|
|
|
ENST00000682869.1:n.2407A>T
(ERCC5)
|
|
|
|
ENST00000683246.1:n.2535A>T
(ERCC5)
|
|
|
|
ENST00000639132.1:c.2433A>T
(BIVM-ERCC5)
|
ENSP00000492684.1:p.Thr811=
|
|
|
ENST00000639435.1:c.3120A>T
(BIVM-ERCC5)
|
ENSP00000491742.1:p.Thr1040=
|
|
|
ENST00000651002.1:c.*1519A>T
(ERCC5)
|
ENSP00000498809.1:n.*1519A>T
|
|
|
ENST00000651055.1:n.1887A>T
(ERCC5)
|
|
|
|
ENST00000651281.1:n.2126A>T
(ERCC5)
|
|
|
|
ENST00000651387.1:n.1242A>T
(ERCC5)
|
|
|
|
ENST00000651470.1:c.1758A>T
(ERCC5)
|
ENSP00000498701.1:p.Thr586=
|
|
|
ENST00000652225.2:c.1758A>T
(ERCC5)
MANE Select
|
ENSP00000498881.2:p.Thr586=
|
|
|
ENST00000652613.1:c.1254A>T
(ERCC5)
|
ENSP00000498357.1:p.Thr418=
|
|
|
ENST00000355739.8:c.1758A>T
(ERCC5)
|
ENSP00000347978.4:p.Thr586=
|
|
|
ENST00000602836.1:c.3034A>T
(BIVM-ERCC5)
|
|
|
|
ENST00000610537.4:c.1758A>T
(ERCC5)
|
ENSP00000478667.1:p.Thr586=
|
|
|
NM_000123.3:c.1758A>T , LRG_464t1:c.1758A>T
(ERCC5)
|
NP_000114.2:p.Thr586=
|
|
|
NM_001204425.1:c.3120A>T
(BIVM-ERCC5)
|
NP_001191354.1:p.Thr1040=
|
|
|
NM_000123.4:c.1758A>T
(ERCC5)
MANE Select
|
NP_000114.3:p.Thr586=
|
|
|
NM_001204425.2:c.3120A>T
(BIVM-ERCC5)
|
NP_001191354.2:p.Thr1040=
|
|
