| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142276.1 | 86 | Intron | NP_001135748.1 | ||
| NM_001142277.1 | 86 | Intron | NP_001135749.1 | ||
| NM_001142278.1 | 86 | Intron | NP_001135750.1 | ||
| NM_001243299.1 | 86 | Missense Mutation | CGC,CTC | R14L | NP_001230228.1 |
| NM_001642.2 | 86 | Intron | NP_001633.1 |