Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_138769.3
p.R261H
c.782G>A
Surrounding Variants
NM_138769.3
p.G262S
c.784G>A
NM_138769.3
p.G262A
c.785G>C
NM_138769.3
p.Q260*
c.778C>T
NM_138769.3
p.I259F
c.775A>T
NM_138769.3
p.G250D
c.749G>A
NM_138769.3
p.G275S
c.823G>A
NM_138769.3
p.T283I
c.848C>T
NM_138769.3
p.G250D
c.749G>A
NM_138769.3
p.R245Q
c.734G>A
NM_138769.3
p.E243G
c.728A>G
NM_138769.3
p.V241G
c.722T>G
NM_138769.3
p.A238V
c.713C>T