Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_001077198.3
p.F46L
c.138C>A
Surrounding Variants
NM_001077198.3
p.F46L
c.138C>G
NM_001077198.3
p.F46L
c.136T>C
NM_001077198.3
p.N42I
c.125A>T
NM_001077198.3
p.I40M
c.120T>G
NM_001077198.3
p.K34M
c.101A>T
NM_001077198.3
p.E31fs
c.91_92fs
NM_001077198.3
p.V27M
c.79G>A
NM_001077198.3
p.Y15F
c.44A>T
NM_001077198.3
p.A13V
c.38C>T
NM_001077198.3
p.Y8F
c.23A>T
NM_001077198.3
p.T6_E7insFs
c.18_19insC
NM_001077198.3
p.A2V
c.5C>T