| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_012339.3 | 129 | Missense Mutation | CCG,TCG | P2S | NP_036471.1 |
| XM_005269666.4 | 129 | Intron | XP_005269723.1 | ||
| XM_005269667.3 | 129 | Missense Mutation | CCG,TCG | P2S | XP_005269724.1 |
| XM_011539562.2 | 129 | Intron | XP_011537864.1 | ||
| XM_011539563.2 | 129 | Intron | XP_011537865.1 | ||
| XM_017016010.1 | 129 | Missense Mutation | CCG,TCG | P2S | XP_016871499.1 |