| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001278211.1 | 654 | Missense Mutation | CCG,CTG | P165L | NP_001265140.1 |
| NM_001278212.1 | 654 | Missense Mutation | CCG,CTG | P165L | NP_001265141.1 |
| NM_001278213.1 | 654 | Missense Mutation | CCG,CTG | P115L | NP_001265142.1 |
| NM_001278214.1 | 654 | Missense Mutation | CCG,CTG | P96L | NP_001265143.1 |
| NM_018205.3 | 654 | Missense Mutation | CCG,CTG | P109L | NP_060675.1 |
| NM_018239.3 | 654 | Missense Mutation | CCG,CTG | P115L | NP_060709.2 |
| NM_207119.2 | 654 | Missense Mutation | CCG,CTG | P165L | NP_997002.1 |
| XM_017016374.1 | 654 | Missense Mutation | CCG,CTG | P165L | XP_016871863.1 |
| XM_017016375.1 | 654 | Missense Mutation | CCG,CTG | P165L | XP_016871864.1 |