Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_001006638.3
p.G76D
c.227G>A
Surrounding Variants
NM_001006638.3
p.A87T
c.259G>A
NM_001006638.3
p.Q89L
c.266A>T
NM_001006638.3
p.R91W
c.271C>T
NM_001006638.3
p.R93*
c.277C>T
NM_001006638.3
p.R93Q
c.278G>A
NM_001006638.3
p.S94R
c.280A>C
NM_001006638.3
p.S94R
c.282C>A
NM_001006638.3
p.S94R
c.282C>G
NM_001006638.3
p.R101K
c.302G>A
NM_001006638.3
p.L108M
c.322C>A
NM_001006638.3
p.S116C
c.347C>G
NM_001006638.3
p.S117C
c.350C>G