| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001185176.1 | 614 | Intron | NP_001172105.1 | ||
| NM_001185177.1 | 614 | Missense Mutation | CGC,TGC | R179C | NP_001172106.1 |
| NM_024922.5 | 614 | Missense Mutation | CGC,TGC | R179C | NP_079198.2 |
| XM_011522975.2 | 614 | Intron | XP_011521277.1 | ||
| XM_011522976.2 | 614 | Missense Mutation | CGC,TGC | R179C | XP_011521278.1 |