Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_001122819.3
p.G754D
c.2261G>A
Surrounding Variants
NM_001122819.3
p.V752F
c.2254G>T
NM_001122819.3
p.L745L
c.2235G>A
NM_001122819.3
p.L763_K764insT
c.2287_2291ins3
NM_001122819.3
p.R769W
c.2305C>T
NM_001122819.3
p.R770C
c.2308C>T
NM_001122819.3
p.A774T
c.2320G>A
NM_001122819.3
p.E776K
c.2326G>A
NM_001122819.3
p.R777C
c.2329C>T
NM_001122819.3
p.R777H
c.2330G>A
NM_001122819.3
p.L785L
c.2355G>A
NM_001122819.3
p.Q786H
c.2358G>T
NM_001122819.3
p.Q786H
c.2358G>C