ENST00000682632.1:n.722G>T
(ERCC5)
|
|
|
ENST00000682869.1:n.1130G>T
(ERCC5)
|
|
|
ENST00000683246.1:n.1258G>T
(ERCC5)
|
|
|
ENST00000684184.1:n.1127G>T
(ERCC5)
|
|
|
ENST00000638434.1:c.579G>T
(BIVM-ERCC5)
|
|
|
ENST00000639132.1:c.1156G>T
(BIVM-ERCC5)
|
ENSP00000492684.1:p.Asp386Tyr
|
|
ENST00000639435.1:c.1843G>T
(BIVM-ERCC5)
|
ENSP00000491742.1:p.Asp615Tyr
|
|
ENST00000651002.1:c.*242G>T
(ERCC5)
|
ENSP00000498809.1:n.*242G>T
|
|
ENST00000651055.1:n.610G>T
(ERCC5)
|
|
|
ENST00000651281.1:n.849G>T
(ERCC5)
|
|
|
ENST00000651470.1:c.481G>T
(ERCC5)
|
ENSP00000498701.1:p.Asp161Tyr
|
|
ENST00000652225.2:c.481G>T
(ERCC5)
MANE Select
|
ENSP00000498881.2:p.Asp161Tyr
|
|
ENST00000652613.1:c.-24G>T
(ERCC5)
|
ENSP00000498357.1:n.-24G>T
|
|
ENST00000355739.8:c.481G>T
(ERCC5)
|
ENSP00000347978.4:p.Asp161Tyr
|
|
ENST00000535557.5:c.481G>T
(ERCC5)
|
ENSP00000442117.1:p.Asp161Tyr
|
|
ENST00000602836.1:c.1757G>T
(BIVM-ERCC5)
|
|
|
ENST00000610537.4:c.481G>T
(ERCC5)
|
ENSP00000478667.1:p.Asp161Tyr
|
|
NM_000123.3:c.481G>T , LRG_464t1:c.481G>T
(ERCC5)
|
NP_000114.2:p.Asp161Tyr
|
|
NM_001204425.1:c.1843G>T
(BIVM-ERCC5)
|
NP_001191354.1:p.Asp615Tyr
|
|
NM_000123.4:c.481G>T
(ERCC5)
MANE Select
|
NP_000114.3:p.Asp161Tyr
|
|
NM_001204425.2:c.1843G>T
(BIVM-ERCC5)
|
NP_001191354.2:p.Asp615Tyr
|
|