Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_000662.8
p.R166T
c.497G>C
Surrounding Variants
NM_000662.8
p.R166G
c.496A>G
NM_000662.8
p.E167K
c.499G>A
NM_000662.8
p.E167Q
c.499G>C
NM_000662.8
p.Y169C
c.506A>G
NM_000662.8
p.I170N
c.509T>A
NM_000662.8
p.L161L
c.481C>T
NM_000662.8
p.N172D
c.514A>G
NM_000662.8
p.E173A
c.518A>C
NM_000662.8
p.W159R
c.475T>A
NM_000662.8
p.W159R
c.475T>C
NM_000662.8
p.F175L
c.523T>C
NM_000662.8
p.F175L
c.525T>A