Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_001077198.3
p.E182D
c.546A>T
Surrounding Variants
NM_001077198.3
p.E182D
c.546A>C
NM_001077198.3
p.V183M
c.547G>A
NM_001077198.3
p.C178Y
c.533G>A
NM_001077198.3
p.I187F
c.559A>T
NM_001077198.3
p.Y177insFs
c.530_531insA
NM_001077198.3
p.L175fs
c.523_524fs
NM_001077198.3
p.K192R
c.575A>G
NM_001077198.3
p.K192K
c.576G>A
NM_001077198.3
p.E193K
c.577G>A
NM_001077198.3
p.M172_S173Splc
c.517-4G>A
NM_001077198.3
p.H199Y
c.595C>T
NM_001077198.3
p.T204A
c.610A>G