Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_001077198.3
p.S592G
c.1774A>G
Surrounding Variants
NM_001077198.3
p.S592I
c.1775G>T
NM_001077198.3
p.L593P
c.1778T>C
NM_001077198.3
p.A594T
c.1780G>A
NM_001077198.3
p.R586Q
c.1757G>A
NM_001077198.3
p.P600S
c.1798C>T
NM_001077198.3
p.K581R
c.1742A>G
NM_001077198.3
p.Q609R
c.1826A>G
NM_001077198.3
p.T574K
c.1721C>A
NM_001077198.3
p.E614G
c.1841A>G
NM_001077198.3
p.T563S
c.1688C>G
NM_001077198.3
p.T563S
c.1687A>T
NM_001077198.3
p.A561D
c.1682C>A