| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001145143.1 | 485 | Missense Mutation | CCT,CTT | P101L | NP_001138615.1 |
| NM_001163646.1 | 485 | Missense Mutation | CCT,CTT | P162L | NP_001157118.1 |
| NM_182537.2 | 485 | Missense Mutation | CCT,CTT | P27L | NP_872343.2 |
| XM_017005854.1 | 485 | Intron | XP_016861343.1 |