Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_000569.8
p.C172W
c.516C>G
Surrounding Variants
NM_000569.8
p.F171C
c.512T>G
NM_000569.8
p.F171Y
c.512T>A
NM_000569.8
p.F176V
c.526T>G
NM_000569.8
p.F176I
c.526T>A
NM_000569.8
p.K179E
c.535A>G
NM_000569.8
p.K165R
c.494A>G
NM_000569.8
p.A162G
c.485C>G
NM_000569.8
p.V186M
c.556G>A
NM_000569.8
p.N187D
c.559A>G
NM_000569.8
p.N187H
c.559A>C
NM_000569.8
p.Y158H
c.472T>C
NM_000569.8
p.G147D
c.440G>A