Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_001077198.3
p.R422W
c.1264A>T
Surrounding Variants
NM_001077198.3
p.R439H
c.1316G>A
NM_001077198.3
p.A443S
c.1327G>T
NM_001077198.3
p.H444P
c.1331A>C
NM_001077198.3
p.A456S
c.1366G>T
NM_001077198.3
p.T461P
c.1381A>C
NM_001077198.3
p.D463D
c.1389C>T
NM_001077198.3
p.H406Y
c.1216C>T
NM_001077198.3
p.V404L
c.1210G>C
NM_001077198.3
p.A403A
c.1209T>A
NM_001077198.3
p.L394P
c.1181T>C
NM_001077198.3
p.I387V
c.1159A>G
NM_001077198.3
p.K378*
c.1132A>T