| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001122847.2 | 2552 | Missense Mutation | ACC,GCC | T598A | NP_001116319.1 |
| NM_001122848.2 | 2552 | Missense Mutation | ACC,GCC | T598A | NP_001116320.1 |
| NM_001206931.1 | 2552 | Missense Mutation | ACC,GCC | T598A | NP_001193860.1 |
| NM_003044.4 | 2552 | Missense Mutation | ACC,GCC | T598A | NP_003035.3 |
| XM_005253747.4 | 2552 | Intron | XP_005253804.1 | ||
| XM_005253748.4 | 2552 | UTR 3 | XP_005253805.1 | ||
| XM_006719005.3 | 2552 | Intron | XP_006719068.1 | ||
| XM_011521010.1 | 2552 | Missense Mutation | ACC,GCC | T598A | XP_011519312.1 |
| XM_017019841.1 | 2552 | Missense Mutation | ACC,GCC | T410A | XP_016875330.1 |