| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001077624.1 | 2353 | Missense Mutation | CCT,CGT | P461R | NP_001071092.1 |
| XM_005259772.3 | 2353 | Missense Mutation | XP_005259829.1 | ||
| XM_005259773.4 | 2353 | Missense Mutation | XP_005259830.1 | ||
| XM_005259775.3 | 2353 | Missense Mutation | XP_005259832.1 | ||
| XM_006722658.3 | 2353 | Intron | XP_006722721.1 | ||
| XM_011527717.2 | 2353 | Missense Mutation | XP_011526019.1 | ||
| XM_011527718.2 | 2353 | Missense Mutation | XP_011526020.1 | ||
| XM_011527719.2 | 2353 | Missense Mutation | XP_011526021.1 | ||
| XM_011527720.2 | 2353 | Missense Mutation | XP_011526022.1 | ||
| XM_011527721.2 | 2353 | Missense Mutation | XP_011526023.1 | ||
| XM_017026404.1 | 2353 | Missense Mutation | XP_016881893.1 | ||
| XM_017026405.1 | 2353 | Missense Mutation | XP_016881894.1 | ||
| XM_017026406.1 | 2353 | Missense Mutation | XP_016881895.1 | ||
| XM_017026407.1 | 2353 | Intron | XP_016881896.1 | ||
| XM_017026408.1 | 2353 | Intron | XP_016881897.1 |