Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000148.3 | 1997 | Missense Mutation | CCG,CTG | P341L | NP_000139.1 |
XM_006723127.2 | 1997 | Missense Mutation | CCG,CTG | P464L | XP_006723190.1 |
XM_017026552.1 | 1997 | Missense Mutation | CCG,CTG | P464L | XP_016882041.1 |
XM_017026553.1 | 1997 | Missense Mutation | CCG,CTG | P341L | XP_016882042.1 |