Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_001077198.3
p.A750V
c.2249C>T
Surrounding Variants
NM_001077198.3
p.R751L
c.2252G>T
NM_001077198.3
p.E748D
c.2244G>T
NM_001077198.3
p.E748D
c.2244G>C
NM_001077198.3
p.G747E
c.2240G>A
NM_001077198.3
p.E745G
c.2234A>G
NM_001077198.3
p.R758C
c.2272C>T
NM_001077198.3
p.A742T
c.2224G>A
NM_001077198.3
p.S741fs
c.2221_2222fs
NM_001077198.3
p.R732H
c.2195G>A
NM_001077198.3
p.T775A
c.2323A>G
NM_001077198.3
p.T775T
c.2325T>C
NM_001077198.3
p.H717Y
c.2149C>T