Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_001069.3
p.M388T
c.1163T>C
Surrounding Variants
NM_001069.3
p.M388V
c.1162A>G
NM_001069.3
p.A387V
c.1160C>T
NM_001069.3
p.R390W
c.1168C>T
NM_001069.3
p.R390Q
c.1169G>A
NM_001069.3
p.R391C
c.1171C>T
NM_001069.3
p.R391H
c.1172G>A
NM_001069.3
p.A393V
c.1178C>T
NM_001069.3
p.H396Y
c.1186C>T
NM_001069.3
p.R380L
c.1139G>T
NM_001069.3
p.R380P
c.1139G>C
NM_001069.3
p.R380C
c.1138C>T
NM_001069.3
p.R380S
c.1138C>A