| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001122890.2 | 1129 | Missense Mutation | ATT,GTT | I384V | NP_001116362.1 |
| NM_001288702.1 | 1129 | Missense Mutation | ATT,GTT | I390V | NP_001275631.1 |
| NM_001288703.1 | 1129 | Missense Mutation | GAT,GGT | D187G | NP_001275632.1 |
| NM_001288704.1 | 1129 | Missense Mutation | GAT,GGT | D155G | NP_001275633.1 |
| NM_153338.3 | 1129 | Missense Mutation | ATT,GTT | I352V | NP_699169.2 |