| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001024644.1 | 968 | Missense Mutation | CGC,TGC | R222C | NP_001019815.1 |
| NM_005283.2 | 968 | Missense Mutation | CGC,TGC | R222C | NP_005274.1 |
| XM_017006196.1 | 968 | Missense Mutation | CGC,TGC | R222C | XP_016861685.1 |
| XM_017006197.1 | 968 | Missense Mutation | CGC,TGC | R222C | XP_016861686.1 |
| XM_017006198.1 | 968 | Missense Mutation | CGC,TGC | R222C | XP_016861687.1 |
| XM_017006199.1 | 968 | Missense Mutation | CGC,TGC | R222C | XP_016861688.1 |
| XM_017006200.1 | 968 | Missense Mutation | CGC,TGC | R222C | XP_016861689.1 |
| XM_017006201.1 | 968 | Missense Mutation | CGC,TGC | R222C | XP_016861690.1 |