Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_000569.8
p.C47W
c.141C>G
Surrounding Variants
NM_000569.8
p.Q48R
c.143A>G
NM_000569.8
p.L45V
c.133C>G
NM_000569.8
p.T44S
c.131C>G
NM_000569.8
p.V43A
c.128T>C
NM_000569.8
p.D41E
c.123C>G
NM_000569.8
p.L38L
c.114C>T
NM_000569.8
p.R36S
c.108G>T
NM_000569.8
p.R36S
c.108G>C
NM_000569.8
p.Q59H
c.177G>T
NM_001127596.2
p.Q58H
c.174G>C
NM_000569.8
p.Q59H
c.177G>C
NM_000569.8
p.E64insFs
c.190_191ins20
NM_000569.8
p.E31Q
c.91G>C