| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001102612.2 | 479 | Missense Mutation | AAG,CAG | K60Q | NP_001096082.2 |
| NM_001167902.1 | 479 | Intron | NP_001161374.1 | ||
| XM_011521254.1 | 479 | Missense Mutation | AAG,CAG | K151Q | XP_011519556.1 |
| XM_017021933.1 | 479 | Missense Mutation | AAG,CAG | K6Q | XP_016877422.1 |