Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_000261.2
p.P16T
c.46C>A
Surrounding Variants
NM_000261.2
p.P16L
c.47C>T
NM_000261.2
p.A17S
c.49G>T
NM_000261.2
p.E14A
c.41A>C
NM_000261.2
p.V18F
c.52G>T
NM_000261.2
p.P13P
c.39T>G
NM_000261.2
p.P13L
c.38C>T
NM_000261.2
p.Q19*
c.55C>T
NM_000261.2
p.Q19K
c.55C>A
NM_000261.2
p.G12G
c.36G>A
NM_000261.2
p.Q19L
c.56A>T
NM_000261.2
p.Q19H
c.57G>T
NM_000261.2
p.Q19H
c.57G>C