| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001308267.1 | 3130 | Silent Mutation | CTG,CTT | L961L | NP_001295196.1 |
| NM_001308268.1 | 3130 | Silent Mutation | CTG,CTT | L1022L | NP_001295197.1 |
| NM_002847.4 | 3130 | Silent Mutation | CTG,CTT | L999L | NP_002838.2 |
| NM_130842.3 | 3130 | Silent Mutation | CTG,CTT | L982L | NP_570857.2 |
| NM_130843.3 | 3130 | Silent Mutation | CTG,CTT | L970L | NP_570858.2 |
| XM_011516446.1 | 3130 | Intron | XP_011514748.1 | ||
| XM_011516447.2 | 3130 | Intron | XP_011514749.1 | ||
| XM_011516448.2 | 3130 | Intron | XP_011514750.1 | ||
| XM_011516449.2 | 3130 | Intron | XP_011514751.1 | ||
| XM_017012475.1 | 3130 | Silent Mutation | CTG,CTT | L933L | XP_016867964.1 |
| XM_017012476.1 | 3130 | Intron | XP_016867965.1 |