| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001205280.1 | 862 | Intron | NP_001192209.1 | ||
| XM_017026317.1 | 862 | Intron | XP_016881806.1 | ||
| XM_017026318.1 | 862 | Intron | XP_016881807.1 | ||
| XM_017026319.1 | 862 | Intron | XP_016881808.1 | ||
| XM_017026320.1 | 862 | Missense Mutation | ACC,GCC | T15A | XP_016881809.1 |
| XM_017026321.1 | 862 | Missense Mutation | ACC,GCC | T15A | XP_016881810.1 |
| XM_017026322.1 | 862 | Missense Mutation | ACC,GCC | T15A | XP_016881811.1 |
| XM_017026323.1 | 862 | Intron | XP_016881812.1 | ||
| XM_017026324.1 | 862 | Intron | XP_016881813.1 | ||
| XM_017026325.1 | 862 | Intron | XP_016881814.1 | ||
| XM_017026326.1 | 862 | Missense Mutation | ACC,GCC | T15A | XP_016881815.1 |