Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_000165.5
p.S296A
c.886T>G
Surrounding Variants
NM_000165.5
p.S296F
c.887C>T
NM_000165.5
p.S297del1
c.889_890delTCT
NM_000165.5
p.S297A
c.889T>G
NM_000165.5
p.N294N
c.882C>T
NM_000165.5
p.C298S
c.892T>A
NM_000165.5
p.R293S
c.879A>T
NM_000165.5
p.C298S
c.893G>C
NM_000165.5
p.R299_N300del2
c.895_899del6
NM_000165.5
p.R299S
c.895C>A
NM_000165.5
p.R299G
c.895C>G
NM_000165.5
p.N300I
c.899A>T
NM_000165.5
p.T290N
c.869C>A