| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_033342.3 | 1500 | Intron | NP_203128.1 | ||
| NM_203293.2 | 1500 | Missense Mutation | ACT,GCT | T476A | NP_976038.1 |
| NM_203294.1 | 1500 | Missense Mutation | ACT,GCT | T268A | NP_976039.1 |
| NM_203295.1 | 1500 | Missense Mutation | ACT,GCT | T268A | NP_976040.1 |
| NM_203296.1 | 1500 | Missense Mutation | ACT,GCT | T268A | NP_976041.1 |
| NM_203297.1 | 1500 | Missense Mutation | ACT,GCT | T294A | NP_976042.1 |
| XM_017009903.1 | 1500 | Missense Mutation | ACT,GCT | T268A | XP_016865392.1 |
| XM_017009904.1 | 1500 | Intron | XP_016865393.1 |