| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001270398.1 | 151 | Missense Mutation | CAC,CCC | H29P | NP_001257327.1 |
| NM_002821.4 | 151 | Intron | NP_002812.2 | ||
| NM_152880.3 | 151 | Intron | NP_690619.1 | ||
| NM_152881.3 | 151 | Intron | NP_690620.1 | ||
| NM_152882.3 | 151 | Intron | NP_690621.1 | ||
| XM_011514765.2 | 151 | Missense Mutation | CAC,CCC | H29P | XP_011513067.1 |
| XM_011514766.2 | 151 | Missense Mutation | CAC,CCC | H29P | XP_011513068.1 |