Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_001077198.3
p.S226P
c.676T>C
Surrounding Variants
NM_001077198.3
p.K225R
c.674A>G
NM_001077198.3
p.K225E
c.673A>G
NM_001077198.3
p.L227R
c.680T>G
NM_001077198.3
p.L222fs
c.664_665fs
NM_001077198.3
p.L230V
c.688C>G
NM_001077198.3
p.F232Y
c.695T>A
NM_001077198.3
p.L237V
c.709C>G
NM_001077198.3
p.G238R
c.712G>C
NM_001077198.3
p.G238R
c.712G>A
NM_001077198.3
p.R211C
c.631C>T
NM_001077198.3
p.L206R
c.617T>G
NM_001077198.3
p.K248*
c.742A>T