Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_001077665.3
p.E584D
c.1752G>C
Surrounding Variants
NM_001077665.3
p.E584D
c.1752G>T
NM_001077665.3
p.Q590H
c.1770G>C
NM_001077665.3
p.Q590H
c.1770G>T
NM_001077665.3
p.T595T
c.1785C>T
NM_001077665.3
p.R565Q
c.1694G>A
NM_001077665.3
p.L642V
c.1924C>G
NM_001077665.3
p.R515C
c.1543C>T
NM_001077665.3
p.S514F
c.1541C>T
NM_001077665.3
p.S508T
c.1523G>C
NM_001077665.3
p.R507insFs
c.1519_1520ins10
NM_001077665.3
p.I505insFs
c.1514_1515ins5
NM_001077665.3
p.S503S
c.1509A>T