| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001319654.1 | 442 | Silent Mutation | CTC,CTT | L22L | NP_001306583.1 |
| NM_001319656.1 | 442 | Silent Mutation | CTC,CTT | L22L | NP_001306585.1 |
| NM_018590.4 | 442 | Silent Mutation | CTC,CTT | L22L | NP_061060.3 |
| XM_011539938.1 | 442 | Silent Mutation | CTC,CTT | L22L | XP_011538240.1 |
| XM_017016388.1 | 442 | Silent Mutation | CTC,CTT | L22L | XP_016871877.1 |
| XM_017016389.1 | 442 | Silent Mutation | CTC,CTT | L22L | XP_016871878.1 |
| XM_017016390.1 | 442 | Silent Mutation | CTC,CTT | L22L | XP_016871879.1 |
| XM_017016391.1 | 442 | Silent Mutation | CTC,CTT | L22L | XP_016871880.1 |