Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_001448.3
p.A442V
c.1325C>T
Surrounding Variants
NM_001448.3
p.G445C
c.1333G>T
NM_001448.3
p.N439insFs
c.1315_1316insC
NM_001448.3
p.F434delins
c.1301_1302delinsTT
NM_001448.3
p.L462R
c.1385T>G
NM_001448.3
p.R463H
c.1388G>A
NM_001448.3
p.S490Splc
c.1469-4C>T
NM_001448.3
p.S490N
c.1469G>A
NM_001448.3
p.E496*
c.1486G>T
NM_001448.3
p.Q506*
c.1516C>T
NM_001448.3
p.P508fs
c.1522_1523fs
NM_001448.3
p.Q506_C507insFs
c.1518_1521dup4
NM_001448.3
p.C507insFs
c.1521dupC