Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_001077628.3
p.M1T
c.2T>C
Surrounding Variants
NM_001077628.3
p.M1I
c.3G>T
NM_001077628.3
p.M1V
c.1A>G
NM_001077628.3
p.V5V
c.15G>A
NM_001077628.3
p.F7L
c.21C>A
NM_001077628.3
p.F11F
c.33C>T
NM_001077628.3
p.V12D
c.35T>A
NM_001077628.3
p.G15A
c.44G>C
NM_001077628.3
p.P16S
c.46C>T
NM_001077628.3
p.P16L
c.47C>T
NM_001077628.3
p.F21L
c.61T>C
NM_001077628.3
p.F21L
c.63C>G
NM_001077628.3
p.F21L
c.63C>A