Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_001077198.3
p.H444P
c.1331A>C
Surrounding Variants
NM_001077198.3
p.A443S
c.1327G>T
NM_001077198.3
p.R439H
c.1316G>A
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.R422W
c.1264A>T
NM_001077198.3
p.A473_V474Splc
c.1420-22G>T
NM_001077198.3
p.V474M
c.1420G>A
NM_001077198.3
p.V474E
c.1421T>A
NM_001077198.3
p.F475F
c.1425C>T
NM_001077198.3
p.H406Y
c.1216C>T
NM_001077198.3
p.V404L
c.1210G>C