| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_032221.4 | 7611 | Missense Mutation | ACA,GCA | T2660A | NP_115597.3 |
| XM_005260573.2 | 7611 | Missense Mutation | ACA,GCA | T2638A | XP_005260630.1 |
| XM_005260576.4 | 7611 | Missense Mutation | ACA,GCA | T1309A | XP_005260633.1 |
| XM_011529080.2 | 7611 | Missense Mutation | ACA,GCA | T2658A | XP_011527382.1 |
| XM_011529082.2 | 7611 | Missense Mutation | ACA,GCA | T1983A | XP_011527384.1 |
| XM_017028099.1 | 7611 | Missense Mutation | ACA,GCA | T2661A | XP_016883588.1 |
| XM_017028100.1 | 7611 | Missense Mutation | ACA,GCA | T2638A | XP_016883589.1 |
| XM_017028101.1 | 7611 | Missense Mutation | ACA,GCA | T2613A | XP_016883590.1 |
| XM_017028102.1 | 7611 | Intron | XP_016883591.1 | ||
| XM_017028103.1 | 7611 | Missense Mutation | ACA,GCA | T2326A | XP_016883592.1 |
| XM_017028104.1 | 7611 | Intron | XP_016883593.1 |