| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001199868.1 | 91 | Missense Mutation | CGC,TGC | R27C | NP_001186797.1 |
| NM_001321980.1 | 91 | Intron | NP_001308909.1 | ||
| NM_006541.4 | 91 | Intron | NP_006532.2 | ||
| XM_017015474.1 | 91 | UTR 5 | XP_016870963.1 |