| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_012434.4 | 1262 | Missense Mutation | ATC,GTC | I442V | NP_036566.1 |
| XM_005248710.3 | 1262 | Missense Mutation | ATC,GTC | I425V | XP_005248767.1 |
| XM_005248711.2 | 1262 | Missense Mutation | ATC,GTC | I376V | XP_005248768.1 |
| XM_011535750.2 | 1262 | Silent Mutation | CCA,CCG | P392P | XP_011534052.1 |
| XM_017010730.1 | 1262 | Missense Mutation | ATC,GTC | I311V | XP_016866219.1 |
| XM_017010731.1 | 1262 | Missense Mutation | ATC,GTC | I311V | XP_016866220.1 |