Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_145270.2 | 1013 | Missense Mutation | CCG,CTG | P245L | NP_660313.1 |
XM_017022959.1 | 1013 | Missense Mutation | CCG,CTG | P245L | XP_016878448.1 |
XM_017022960.1 | 1013 | Missense Mutation | CCG,CTG | P245L | XP_016878449.1 |
XM_017022961.1 | 1013 | Intron | XP_016878450.1 |