Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_000789.4
p.W227C
c.681G>C
Surrounding Variants
NM_000789.4
p.W227*
c.681G>A
NM_000789.4
p.R228C
c.682C>T
NM_000789.4
p.W227L
c.680G>T
NM_000789.4
p.R228H
c.683G>A
NM_000789.4
p.W227R
c.679T>A
NM_000789.4
p.W227R
c.679T>C
NM_000789.4
p.S229F
c.686C>T
NM_000789.4
p.Y226N
c.676T>A
NM_000789.4
p.Y226H
c.676T>C
NM_000789.4
p.A225_Y226Fs
c.675_676delinsGFs
NM_000789.4
p.A225V
c.674C>T
NM_000789.4
p.W230*
c.689G>A