| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000541.4 | 112 | Missense Mutation | CCG,CTG | P12L | NP_000532.2 |
| XM_011511593.2 | 112 | Intron | XP_011509895.1 | ||
| XM_011511594.1 | 112 | Intron | XP_011509896.1 | ||
| XM_011511596.1 | 112 | Intron | XP_011509898.1 | ||
| XM_017004641.1 | 112 | Missense Mutation | CCG,CTG | P12L | XP_016860130.1 |
| XM_017004642.1 | 112 | Missense Mutation | CCG,CTG | P12L | XP_016860131.1 |
| XM_017004643.1 | 112 | Missense Mutation | CCG,CTG | P12L | XP_016860132.1 |