| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_020971.2 | 239 | Missense Mutation | CGC,CTC | R24L | NP_066022.2 |
| NM_025213.2 | 239 | Intron | NP_079489.2 | ||
| XM_011527173.2 | 239 | Missense Mutation | CGC,CTC | R24L | XP_011525475.1 |
| XM_017027049.1 | 239 | Missense Mutation | CGC,CTC | R24L | XP_016882538.1 |
| XM_017027050.1 | 239 | Intron | XP_016882539.1 | ||
| XM_017027051.1 | 239 | Missense Mutation | CGC,CTC | R24L | XP_016882540.1 |
| XM_017027052.1 | 239 | Missense Mutation | CGC,CTC | R24L | XP_016882541.1 |