| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001316345.1 | 126 | UTR 5 | NP_001303274.1 | ||
| NM_001316346.1 | 126 | Missense Mutation | CCC,CTC | P13L | NP_001303275.1 |
| NM_001316347.1 | 126 | Missense Mutation | CCC,CTC | P13L | NP_001303276.1 |
| NM_001316348.1 | 126 | Missense Mutation | CCC,CTC | P13L | NP_001303277.1 |
| NM_021111.2 | 126 | Missense Mutation | CCC,CTC | P13L | NP_066934.1 |
| XM_017015207.1 | 126 | UTR 5 | XP_016870696.1 | ||
| XM_017015208.1 | 126 | UTR 5 | XP_016870697.1 | ||
| XM_017015209.1 | 126 | UTR 5 | XP_016870698.1 | ||
| XM_017015210.1 | 126 | Intron | XP_016870699.1 | ||
| XM_017015211.1 | 126 | Missense Mutation | CCC,CTC | P13L | XP_016870700.1 |