| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001004105.2 | 307 | Silent Mutation | CTC,CTT | L49L | NP_001004105.1 |
| NM_001004106.2 | 307 | Silent Mutation | CTC,CTT | L49L | NP_001004106.1 |
| NM_002082.3 | 307 | Silent Mutation | CTC,CTT | L49L | NP_002073.2 |
| XM_006714858.3 | 307 | Intron | XP_006714921.1 | ||
| XM_006714859.2 | 307 | Silent Mutation | CTC,CTT | L17L | XP_006714922.1 |
| XM_011534537.2 | 307 | Missense Mutation | TCG,TTG | S48L | XP_011532839.1 |
| XM_011534538.1 | 307 | Intron | XP_011532840.1 |