Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_001076678.3
p.I764T
c.2291T>C
Surrounding Variants
NM_001076678.3
p.H763N
c.2287C>A
NM_001076678.3
p.H763D
c.2287C>G
NM_001076678.3
p.A745E
c.2234C>A
NM_001076678.3
p.Y741C
c.2222A>G
NM_001076678.3
p.D738E
c.2214C>A
NM_001076678.3
p.D738E
c.2214C>G
NM_001076678.3
p.L733I
c.2197C>A
NM_001076678.3
p.C713Y
c.2138G>A
NM_001076678.3
p.R696*
c.2086C>T
NM_001076678.3
p.K689E
c.2065A>G
NM_001076678.3
p.E681G
c.2042A>G
NM_001076678.3
p.S652_V653insFs
c.1956_1957insA