| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001277731.1 | 1185 | Missense Mutation | CGC,TGC | R322C | NP_001264660.1 |
| NM_001277732.1 | 1185 | Intron | NP_001264661.1 | ||
| NM_003734.3 | 1185 | Missense Mutation | CGC,TGC | R322C | NP_003725.1 |
| XM_011525419.1 | 1185 | Missense Mutation | CGC,TGC | R322C | XP_011523721.1 |
| XM_011525420.2 | 1185 | Missense Mutation | CGC,TGC | R322C | XP_011523722.1 |