| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015533.3 | 491 | Missense Mutation | CGC,CTC | R35L | NP_056348.2 |
| XM_011544912.2 | 491 | Missense Mutation | CGC,CTC | R81L | XP_011543214.1 |
| XM_017017517.1 | 491 | Missense Mutation | CGC,CTC | R81L | XP_016873006.1 |
| XM_017017518.1 | 491 | Missense Mutation | CGC,CTC | R81L | XP_016873007.1 |
| XM_017017519.1 | 491 | Missense Mutation | CGC,CTC | R35L | XP_016873008.1 |
| XM_017017520.1 | 491 | Missense Mutation | CGC,CTC | R81L | XP_016873009.1 |
| XM_017017521.1 | 491 | Missense Mutation | CGC,CTC | R35L | XP_016873010.1 |
| XM_017017522.1 | 491 | Missense Mutation | CGC,CTC | R35L | XP_016873011.1 |
| XM_017017523.1 | 491 | Missense Mutation | CGC,CTC | R35L | XP_016873012.1 |
| XM_017017524.1 | 491 | UTR 5 | XP_016873013.1 |