Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_175734.4 | 615 | Missense Mutation | CCG,CTG | P181L | NP_783861.3 |
XM_006721471.3 | 615 | Missense Mutation | CCG,CTG | P84L | XP_006721534.1 |
XM_011523722.2 | 615 | Missense Mutation | CCG,CTG | P15L | XP_011522024.1 |