Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_014963.3
p.T577A
c.1729A>G
Surrounding Variants
NM_014963.3
p.H592H
c.1776C>T
NM_014963.3
p.V597D
c.1790T>A
NM_014963.3
p.R554C
c.1660C>T
NM_014963.3
p.L532M
c.1594C>A
NM_014963.3
p.S528A
c.1582T>G
NM_014963.3
p.A511G
c.1532C>G
NM_014963.3
p.R629Splc
c.1885+168G>A
NM_014963.3
p.A498insFs
c.1493_1494ins14
NM_014963.3
p.E492del1
c.1474_1476delCTC
NM_014963.3
p.A462T
c.1384G>A
NM_014963.3
p.R458Splc
c.1374-43C>T
NM_014963.3
p.G633A
c.1898G>C