ENST00000682632.1:n.4035T>C
(ERCC5)
|
|
|
ENST00000682869.1:n.3583T>C
(ERCC5)
|
|
|
ENST00000683246.1:n.4571T>C
(ERCC5)
|
|
|
ENST00000683642.1:n.3164T>C
(ERCC5)
|
|
|
ENST00000639132.1:c.3609T>C
(BIVM-ERCC5)
|
ENSP00000492684.1:p.Phe1203=
|
|
ENST00000639435.1:c.4296T>C
(BIVM-ERCC5)
|
ENSP00000491742.1:p.Phe1432=
|
|
ENST00000651002.1:c.*2695T>C
(ERCC5)
|
ENSP00000498809.1:n.*2695T>C
|
|
ENST00000651055.1:n.3061T>C
(ERCC5)
|
|
|
ENST00000651281.1:n.3302T>C
(ERCC5)
|
|
|
ENST00000651387.1:n.2418T>C
(ERCC5)
|
|
|
ENST00000651470.1:c.*106T>C
(ERCC5)
|
ENSP00000498701.1:n.*106T>C
|
|
ENST00000652225.2:c.2934T>C
(ERCC5)
MANE Select
|
ENSP00000498881.2:p.Phe978=
|
|
ENST00000652613.1:c.2430T>C
(ERCC5)
|
ENSP00000498357.1:p.Phe810=
|
|
ENST00000355739.8:c.2934T>C
(ERCC5)
|
ENSP00000347978.4:p.Phe978=
|
|
ENST00000375954.1:c.633T>C
(ERCC5)
|
ENSP00000365121.1:p.Phe211=
|
|
ENST00000610537.4:c.2931T>C
(ERCC5)
|
ENSP00000478667.1:p.Phe977=
|
|
NM_000123.3:c.2934T>C , LRG_464t1:c.2934T>C
(ERCC5)
|
NP_000114.2:p.Phe978=
|
|
NM_001204425.1:c.4296T>C
(BIVM-ERCC5)
|
NP_001191354.1:p.Phe1432=
|
|
NM_000123.4:c.2934T>C
(ERCC5)
MANE Select
|
NP_000114.3:p.Phe978=
|
|
NM_001204425.2:c.4296T>C
(BIVM-ERCC5)
|
NP_001191354.2:p.Phe1432=
|
|