| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001163812.1 | 973 | Missense Mutation | CTT,GTT | L267V | NP_001157284.1 |
| NM_001163813.1 | 973 | Intron | NP_001157285.1 | ||
| NM_001163814.1 | 973 | Intron | NP_001157286.1 | ||
| NM_021830.4 | 973 | Missense Mutation | CTT,GTT | L267V | NP_068602.2 |
| XM_011539975.2 | 973 | Intron | XP_011538277.1 | ||
| XM_017016437.1 | 973 | UTR 5 | XP_016871926.1 |