Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_000765.5
p.T409R
c.1226C>G
Surrounding Variants
NM_000765.5
p.P416L
c.1247C>T
NM_000765.5
p.H402Y
c.1204C>T
NM_000765.5
p.E417K
c.1249G>A
NM_000765.5
p.E417D
c.1251A>C
NM_000765.5
p.M395V
c.1183A>G
NM_000765.5
p.G391V
c.1172G>T
NM_000765.5
p.I388V
c.1162A>G
NM_000765.5
p.E374D
c.1122G>T
NM_000765.5
p.E374D
c.1122G>C
NM_000765.5
p.L373F
c.1117C>T
NM_000765.5
p.R372K
c.1115G>A
NM_000765.5
p.A370T
c.1108G>A