| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001013838.1 | 602 | Missense Mutation | CCT,CTT | P120L | NP_001013860.1 |
| NM_001317026.1 | 602 | Missense Mutation | CCT,CTT | P120L | NP_001303955.1 |
| XM_011522874.1 | 602 | Missense Mutation | CCT,CTT | P120L | XP_011521176.1 |
| XM_011522875.2 | 602 | Missense Mutation | CCT,CTT | P120L | XP_011521177.2 |
| XM_017022953.1 | 602 | Missense Mutation | CCT,CTT | P120L | XP_016878442.1 |