| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001025081.1 | 639 | Missense Mutation | ACG,ATG | T194M | NP_001020252.1 |
| NM_001025090.1 | 639 | Missense Mutation | ACG,ATG | T168M | NP_001020261.1 |
| NM_001025092.1 | 639 | Missense Mutation | ACG,ATG | T157M | NP_001020263.1 |
| NM_001025100.1 | 639 | Intron | NP_001020271.1 | ||
| NM_001025101.1 | 639 | Missense Mutation | ACG,ATG | T301M | NP_001020272.1 |
| NM_002385.2 | 639 | Missense Mutation | ACG,ATG | T183M | NP_002376.1 |
| XM_011526009.2 | 639 | Intron | XP_011524311.1 | ||
| XM_017025778.1 | 639 | Intron | XP_016881267.1 | ||
| XM_017025779.1 | 639 | Intron | XP_016881268.1 | ||
| XM_017025780.1 | 639 | Intron | XP_016881269.1 |