| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001199809.1 | 2660 | Silent Mutation | CTG,TTG | L778L | NP_001186738.1 |
| NM_001199811.1 | 2660 | Silent Mutation | CTG,TTG | L813L | NP_001186740.1 |
| NM_001199812.1 | 2660 | Silent Mutation | CTG,TTG | L807L | NP_001186741.1 |
| NM_015434.3 | 2660 | Silent Mutation | CTG,TTG | L827L | NP_056249.1 |
| XM_011509396.2 | 2660 | Silent Mutation | CTG,TTG | L863L | XP_011507698.1 |
| XM_017000962.1 | 2660 | Intron | XP_016856451.1 |