| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_004178.4 | 535 | Missense Mutation | CCC,CGC | P122R | NP_004169.3 |
| NM_134323.1 | 535 | Missense Mutation | CCC,CGC | P143R | NP_599150.1 |
| NM_134324.2 | 535 | Missense Mutation | CCC,CGC | P122R | NP_599151.2 |
| XM_005269114.1 | 535 | Missense Mutation | CCC,CGC | P122R | XP_005269171.1 |
| XM_005269115.2 | 535 | Missense Mutation | CCC,CGC | P122R | XP_005269172.1 |
| XM_005269117.1 | 535 | Missense Mutation | CCC,CGC | P143R | XP_005269174.1 |
| XM_005269120.4 | 535 | UTR 5 | XP_005269177.1 | ||
| XM_005269122.3 | 535 | UTR 5 | XP_005269179.1 | ||
| XM_006719581.1 | 535 | Missense Mutation | CCC,CGC | P44R | XP_006719644.1 |
| XM_011538712.2 | 535 | UTR 5 | XP_011537014.1 | ||
| XM_017019910.1 | 535 | Missense Mutation | CCC,CGC | P122R | XP_016875399.1 |
| XM_017019911.1 | 535 | UTR 5 | XP_016875400.1 |