| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_018356.2 | 618 | Missense Mutation | GCT,GGT | A104G | NP_060826.2 |
| XM_006714479.2 | 618 | Missense Mutation | GCT,GGT | A20G | XP_006714542.1 |
| XM_006714480.3 | 618 | UTR 5 | XP_006714543.1 | ||
| XM_011514062.2 | 618 | Missense Mutation | GCT,GGT | A135G | XP_011512364.1 |
| XM_017009607.1 | 618 | Missense Mutation | GCT,GGT | A135G | XP_016865096.1 |
| XM_017009608.1 | 618 | Missense Mutation | GCT,GGT | A104G | XP_016865097.1 |
| XM_017009609.1 | 618 | Missense Mutation | GCT,GGT | A20G | XP_016865098.1 |
| XM_017009610.1 | 618 | UTR 5 | XP_016865099.1 | ||
| XM_017009611.1 | 618 | UTR 5 | XP_016865100.1 | ||
| XM_017009612.1 | 618 | UTR 5 | XP_016865101.1 | ||
| XM_017009613.1 | 618 | UTR 5 | XP_016865102.1 | ||
| XM_017009614.1 | 618 | UTR 5 | XP_016865103.1 | ||
| XM_017009615.1 | 618 | UTR 5 | XP_016865104.1 | ||
| XM_017009616.1 | 618 | UTR 5 | XP_016865105.1 |