Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_001122819.3
p.C885C
c.2655C>T
Surrounding Variants
NM_001122819.3
p.R882H
c.2645G>A
NM_001122819.3
p.R882C
c.2644C>T
NM_001122819.3
p.G891D
c.2672G>A
NM_001122819.3
p.F892L
c.2674T>C
NM_001122819.3
p.F892L
c.2676C>G
NM_001122819.3
p.F892L
c.2676C>A
NM_001122819.3
p.L877L
c.2631G>A
NM_001122819.3
p.V899I
c.2695G>A
NM_001122819.3
p.R869C
c.2605C>T
NM_001122819.3
p.S904R
c.2710A>C
NM_001122819.3
p.S904R
c.2712C>G
NM_001122819.3
p.S904R
c.2712C>A