| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001101362.2 | 115 | Missense Mutation | CGC,GGC | R39G | NP_001094832.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001307930.1 | 115 | Intron | NP_001294859.1 | ||
| NM_016563.3 | 115 | Intron | NP_057647.1 | ||
| XM_005254434.4 | 115 | Intron | XP_005254491.1 | ||
| XM_011521660.2 | 115 | Intron | XP_011519962.1 | ||
| XM_017022296.1 | 115 | Intron | XP_016877785.1 |