Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_000137.4
p.W262S
c.785G>C
Surrounding Variants
NM_000137.4
p.W262*
c.785G>A
NM_000137.4
p.W262*
c.786G>A
NM_000137.4
p.V263M
c.787G>A
NM_000137.4
p.V263fs
c.787_788fs
NM_000137.4
p.V263delFs
c.788delT
NM_000137.4
p.P261L
c.782C>T
NM_000137.4
p.V259D
c.776T>A
NM_000137.4
p.V259L
c.775G>C
NM_000137.4
p.M266V
c.796A>G
NM_000137.4
p.M266I
c.798G>C
NM_000137.4
p.A268D
c.803C>A
NM_000137.4
p.G256W
c.766G>T