| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001242729.1 | 237 | Missense Mutation | CTC,GTC | L26V | NP_001229658.1 |
| NM_017700.1 | 237 | Missense Mutation | CTC,GTC | L26V | NP_060170.1 |
| XM_006714244.3 | 237 | Intron | XP_006714307.1 | ||
| XM_011532050.2 | 237 | Intron | XP_011530352.1 | ||
| XM_011532051.2 | 237 | Missense Mutation | CTC,GTC | L26V | XP_011530353.1 |