Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_001167856.3
p.S729N
c.2186G>A
Surrounding Variants
NM_001167856.3
p.S728N
c.2183G>A
NM_001167856.3
p.G724C
c.2170G>T
NM_001167856.3
p.S740F
c.2219C>T
NM_001167856.3
p.W777L
c.2330G>T
NM_001167856.3
p.K790fs
c.2368_2369fs
NM_001167856.3
p.K790delFs
c.2369delT
NM_001167856.3
p.K792E
c.2374A>G
NM_001167856.3
p.G883V
c.2648G>T
NM_001167856.3
p.N886K
c.2658C>G
NM_001167856.3
p.N886K
c.2658C>A
NM_001167856.3
p.E889_M890Splc
c.2668-14G>A
NM_001167856.3
p.G709Splc
c.2125+2T>C