| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001289112.1 | 3300 | Missense Mutation | CCA,CTA | P575L | NP_001276041.1 |
| NM_130808.2 | 3300 | Missense Mutation | CCA,CTA | P557L | NP_570720.1 |
| NM_153429.1 | 3300 | Missense Mutation | CCA,CTA | P575L | NP_702907.1 |
| XM_011512406.2 | 3300 | Missense Mutation | CCA,CTA | P444L | XP_011510708.1 |
| XM_011512407.2 | 3300 | Missense Mutation | CCA,CTA | P444L | XP_011510709.1 |
| XM_011512408.2 | 3300 | Missense Mutation | CCA,CTA | P444L | XP_011510710.1 |
| XM_017005693.1 | 3300 | Missense Mutation | CCA,CTA | P575L | XP_016861182.1 |
| XM_017005694.1 | 3300 | Intron | XP_016861183.1 | ||
| XM_017005695.1 | 3300 | Missense Mutation | CCA,CTA | P417L | XP_016861184.1 |
| XM_017005696.1 | 3300 | Missense Mutation | CCA,CTA | P306L | XP_016861185.1 |