| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001256378.1 | 1687 | Missense Mutation | CCG,CTG | P514L | NP_001243307.1 |
| NM_001256379.1 | 1687 | Missense Mutation | CCG,CTG | P341L | NP_001243308.1 |
| NM_024834.3 | 1687 | Missense Mutation | CCG,CTG | P516L | NP_079110.1 |
| XM_005270157.4 | 1687 | Missense Mutation | CCG,CTG | P516L | XP_005270214.1 |
| XM_011540170.1 | 1687 | Missense Mutation | CCG,CTG | P446L | XP_011538472.1 |
| XM_017016663.1 | 1687 | Missense Mutation | CCG,CTG | P514L | XP_016872152.1 |
| XM_017016664.1 | 1687 | Missense Mutation | CCG,CTG | P444L | XP_016872153.1 |