Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_000796.6
p.Y13F
c.38A>T
Surrounding Variants
NM_000796.6
p.H10insFs
c.29_30insTC
NM_000796.6
p.G16G
c.48G>A
NM_000796.6
p.A17V
c.50C>T
NM_000796.6
p.G9S
c.25G>A
NM_000796.6
p.T21A
c.61A>G
NM_000796.6
p.T21R
c.62C>G
NM_000796.6
p.G22G
c.66T>A
NM_000796.6
p.S3S
c.9T>C
NM_000796.6
p.S24S
c.72C>T
NM_000796.6
p.M1K
c.2T>A
NM_000796.6
p.H29Y
c.85C>T
NM_000796.6
p.Y32H
c.94T>C