Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_000261.2
p.G374V
c.1121G>T
Surrounding Variants
NM_000261.2
p.W373C
c.1119G>T
NM_000261.2
p.W373C
c.1119G>C
NM_000261.2
p.W373*
c.1119G>A
NM_000261.2
p.W373L
c.1118G>T
NM_000261.2
p.W373*
c.1118G>A
NM_000261.2
p.S372C
c.1115C>G
NM_000261.2
p.S372Y
c.1115C>A
NM_000261.2
p.T377A
c.1129A>G
NM_000261.2
p.T377M
c.1130C>T
NM_000261.2
p.T377R
c.1130C>G
NM_000261.2
p.T377K
c.1130C>A
NM_000261.2
p.Y371D
c.1111T>G