| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001010860.1 | 119 | Missense Mutation | ACG,ATG | T40M | NP_001010860.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_213601.1 | 119 | Intron | NP_998766.1 | ||
| XM_017021223.1 | 119 | Intron | XP_016876712.1 | ||
| XM_017021224.1 | 119 | Intron | XP_016876713.1 | ||
| XM_017021225.1 | 119 | Intron | XP_016876714.1 |