| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_004119.2 | 2865 | Missense Mutation | CGT,GGT | R961G | NP_004110.2 |
| XM_011535015.2 | 2865 | Missense Mutation | CGT,GGT | R942G | XP_011533317.1 |
| XM_011535017.2 | 2865 | Missense Mutation | CGT,GGT | R786G | XP_011533319.1 |
| XM_011535018.2 | 2865 | Missense Mutation | CGT,GGT | R786G | XP_011533320.1 |
| XM_017020486.1 | 2865 | Missense Mutation | CGT,GGT | R889G | XP_016875975.1 |
| XM_017020487.1 | 2865 | Missense Mutation | CGT,GGT | R786G | XP_016875976.1 |
| XM_017020488.1 | 2865 | Missense Mutation | CGT,GGT | R668G | XP_016875977.1 |
| XM_017020489.1 | 2865 | Missense Mutation | CGT,GGT | R662G | XP_016875978.1 |