| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001177663.1 | 64 | Missense Mutation | CCC,CTC | P8L | NP_001171134.1 |
| NM_001177664.1 | 64 | Missense Mutation | CCC,CTC | P8L | NP_001171135.1 |
| NM_001177665.1 | 64 | Missense Mutation | CCC,CTC | P8L | NP_001171136.1 |
| NM_018151.4 | 64 | Missense Mutation | CCC,CTC | P8L | NP_060621.3 |
| XM_005246665.3 | 64 | Missense Mutation | CCC,CTC | P8L | XP_005246722.1 |
| XM_011511395.2 | 64 | Missense Mutation | CCC,CTC | P8L | XP_011509697.1 |
| XM_017004422.1 | 64 | Missense Mutation | CCC,CTC | P8L | XP_016859911.1 |
| XM_017004423.1 | 64 | Missense Mutation | CCC,CTC | P8L | XP_016859912.1 |
| XM_017004424.1 | 64 | Intron | XP_016859913.1 | ||
| XM_017004425.1 | 64 | Missense Mutation | CCC,CTC | P8L | XP_016859914.1 |