| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142497.2 | 2031 | Missense Mutation | ATT,CTT | I237L | NP_001135969.1 |
| NM_152649.3 | 2031 | Missense Mutation | ATT,CTT | I445L | NP_689862.1 |
| XM_005255834.3 | 2031 | Missense Mutation | ATT,CTT | I445L | XP_005255891.1 |
| XM_011522936.2 | 2031 | Intron | XP_011521238.1 |