| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001006109.1 | 191 | Missense Mutation | CCC,CTC | P29L | NP_001006109.1 |
| NM_020187.2 | 191 | Missense Mutation | CCC,CTC | P29L | NP_064572.2 |
| XM_005247636.3 | 191 | Missense Mutation | CCC,CTC | P29L | XP_005247693.1 |
| XM_005247637.3 | 191 | Missense Mutation | CCC,CTC | P29L | XP_005247694.1 |
| XM_017006877.1 | 191 | Missense Mutation | CCC,CTC | P29L | XP_016862366.1 |