| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001010895.2 | 429 | Missense Mutation | CAG,CCG | Q14P | NP_001010895.1 |
| NM_020207.4 | 429 | Missense Mutation | CAG,CCG | Q14P | NP_064592.2 |
| XM_011518641.2 | 429 | Missense Mutation | CAG,CCG | Q14P | XP_011516943.1 |
| XM_011518644.2 | 429 | UTR 5 | XP_011516946.1 | ||
| XM_011518645.2 | 429 | Missense Mutation | CAG,CCG | Q14P | XP_011516947.1 |
| XM_011518646.2 | 429 | Missense Mutation | CAG,CCG | Q14P | XP_011516948.1 |
| XM_011518647.1 | 429 | Missense Mutation | CAG,CCG | Q14P | XP_011516949.1 |
| XM_011518648.2 | 429 | Intron | XP_011516950.1 | ||
| XM_011518650.2 | 429 | Intron | XP_011516952.1 | ||
| XM_017014707.1 | 429 | UTR 5 | XP_016870196.1 |