Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001013743.2 | 802 | Missense Mutation | CGT,GGT | R110G | NP_001013765.2 |
XM_006718832.3 | 802 | Missense Mutation | CGT,GGT | R60G | XP_006718895.1 |
XM_011542802.2 | 802 | Missense Mutation | CGA,GGA | R110G | XP_011541104.1 |
XM_017017653.1 | 802 | Missense Mutation | CTT,GTT | L110V | XP_016873142.1 |