Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_052899.3
p.A898G
c.2693C>G
Surrounding Variants
NM_052899.3
p.A902V
c.2705C>T
NM_052899.3
p.P904insFs
c.2710_2711insT
NM_052899.3
p.G894_P903del10
c.2680_2708del30
NM_052899.3
p.P904L
c.2711C>T
NM_052899.3
p.P904fs
c.2710_2711fs
NM_052899.3
p.E905_P906insFs
c.2715_2716insTC
NM_052899.3
p.P906fs
c.2716_2717fs
NM_052899.3
p.E888*
c.2662G>T
NM_052899.3
p.P887L
c.2660C>T
NM_052899.3
p.P887T
c.2659C>A
NM_052899.3
p.A881T
c.2641G>A
NM_052899.3
p.D916N
c.2746G>A