| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001184957.1 | 496 | Intron | NP_001171886.1 | ||
| NM_001184958.1 | 496 | Intron | NP_001171887.1 | ||
| NM_032137.4 | 496 | Missense Mutation | ACA,ATA | T15I | NP_115513.4 |
| XM_006713341.2 | 496 | Missense Mutation | ACA,ATA | T15I | XP_006713404.1 |
| XM_006713342.2 | 496 | Missense Mutation | ACA,ATA | T15I | XP_006713405.1 |
| XM_006713343.2 | 496 | Missense Mutation | ACA,ATA | T15I | XP_006713406.1 |
| XM_011534153.2 | 496 | Missense Mutation | ACA,ATA | T15I | XP_011532455.1 |
| XM_011534154.2 | 496 | Intron | XP_011532456.1 | ||
| XM_011534157.2 | 496 | Intron | XP_011532459.1 | ||
| XM_011534158.2 | 496 | Missense Mutation | ACA,ATA | T15I | XP_011532460.1 |
| XM_017007310.1 | 496 | Missense Mutation | ACA,ATA | T15I | XP_016862799.1 |