| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001317824.1 | 440 | Intron | NP_001304753.1 | ||
| NM_001317825.1 | 440 | Missense Mutation | ACC,GCC | T5A | NP_001304754.1 |
| NM_001317826.1 | 440 | Missense Mutation | ACC,GCC | T68A | NP_001304755.1 |
| NM_017872.4 | 440 | Missense Mutation | ACC,GCC | T130A | NP_060342.2 |
| XM_017009603.1 | 440 | Intron | XP_016865092.1 |