| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001281303.1 | 1494 | Missense Mutation | CAT,CGT | H453R | NP_001268232.1 |
| NM_006415.3 | 1494 | Missense Mutation | ATC,GTC | I464V | NP_006406.1 |
| NM_178324.2 | 1494 | Intron | NP_847894.1 | ||
| XM_011518138.2 | 1494 | Intron | XP_011516440.1 | ||
| XM_011518139.2 | 1494 | Missense Mutation | ATC,GTC | I309V | XP_011516441.1 |
| XM_017014200.1 | 1494 | Missense Mutation | ATC,GTC | I342V | XP_016869689.1 |
| XM_017014201.1 | 1494 | Missense Mutation | ATC,GTC | I342V | XP_016869690.1 |
| XM_017014202.1 | 1494 | Missense Mutation | ATC,GTC | I337V | XP_016869691.1 |