Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_004762.6
p.R281C
c.841C>T
Surrounding Variants
NM_004762.6
p.T277A
c.829A>G
NM_004762.6
p.P261S
c.781C>T
NM_004762.6
p.E248K
c.742G>A
NM_004762.6
p.R213delFs
c.639delC
NM_004762.6
p.E212K
c.634G>A
NM_004762.6
p.S199N
c.596G>A
NM_004762.6
p.T183T
c.549G>T
NM_004762.6
p.Q170*
c.508C>T
NM_004762.6
p.E157K
c.469G>A
NM_004762.6
p.A144delFs
c.431_432delTG
NM_004762.6
p.V142F
c.424G>T
NM_004762.6
p.V142I
c.424G>A