| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_014951.2 | 949 | Missense Mutation | CCG,CTG | P29L | NP_055766.2 |
| NM_199450.2 | 949 | Missense Mutation | CCG,CTG | P29L | NP_955522.1 |
| NM_199451.2 | 949 | Missense Mutation | CCG,CTG | P29L | NP_955523.1 |
| NM_199452.3 | 949 | Intron | NP_955524.3 | ||
| XM_017015937.1 | 949 | Missense Mutation | CCG,CTG | P29L | XP_016871426.1 |
| XM_017015938.1 | 949 | Intron | XP_016871427.1 | ||
| XM_017015939.1 | 949 | Intron | XP_016871428.1 | ||
| XM_017015940.1 | 949 | Intron | XP_016871429.1 | ||
| XM_017015941.1 | 949 | Intron | XP_016871430.1 |