ENST00000682632.1:n.3998T>A
(ERCC5)
|
|
|
ENST00000682869.1:n.3546T>A
(ERCC5)
|
|
|
ENST00000683246.1:n.4534T>A
(ERCC5)
|
|
|
ENST00000683642.1:n.3127T>A
(ERCC5)
|
|
|
ENST00000639132.1:c.3572T>A
(BIVM-ERCC5)
|
ENSP00000492684.1:p.Phe1191Tyr
|
|
ENST00000639435.1:c.4259T>A
(BIVM-ERCC5)
|
ENSP00000491742.1:p.Phe1420Tyr
|
|
ENST00000651002.1:c.*2658T>A
(ERCC5)
|
ENSP00000498809.1:n.*2658T>A
|
|
ENST00000651055.1:n.3024T>A
(ERCC5)
|
|
|
ENST00000651281.1:n.3265T>A
(ERCC5)
|
|
|
ENST00000651387.1:n.2381T>A
(ERCC5)
|
|
|
ENST00000651470.1:c.*69T>A
(ERCC5)
|
ENSP00000498701.1:n.*69T>A
|
|
ENST00000652225.2:c.2897T>A
(ERCC5)
MANE Select
|
ENSP00000498881.2:p.Phe966Tyr
|
|
ENST00000652613.1:c.2393T>A
(ERCC5)
|
ENSP00000498357.1:p.Phe798Tyr
|
|
ENST00000355739.8:c.2897T>A
(ERCC5)
|
ENSP00000347978.4:p.Phe966Tyr
|
|
ENST00000375954.1:c.596T>A
(ERCC5)
|
ENSP00000365121.1:p.Phe199Tyr
|
|
ENST00000610537.4:c.2894T>A
(ERCC5)
|
ENSP00000478667.1:p.Phe965Tyr
|
|
NM_000123.3:c.2897T>A , LRG_464t1:c.2897T>A
(ERCC5)
|
NP_000114.2:p.Phe966Tyr
|
|
NM_001204425.1:c.4259T>A
(BIVM-ERCC5)
|
NP_001191354.1:p.Phe1420Tyr
|
|
NM_000123.4:c.2897T>A
(ERCC5)
MANE Select
|
NP_000114.3:p.Phe966Tyr
|
|
NM_001204425.2:c.4259T>A
(BIVM-ERCC5)
|
NP_001191354.2:p.Phe1420Tyr
|
|