| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001282957.1 | 324 | Missense Mutation | CCG,CTG | P32L | NP_001269886.1 |
| NM_207417.2 | 324 | Missense Mutation | CCG,CTG | P32L | NP_997300.1 |
| XM_011518670.2 | 324 | Missense Mutation | CCG,CTG | P32L | XP_011516972.1 |
| XM_011518671.1 | 324 | Missense Mutation | CCG,CTG | P32L | XP_011516973.1 |
| XM_017014711.1 | 324 | Missense Mutation | CCG,CTG | P32L | XP_016870200.1 |