Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006500.2 | 1836 | Missense Mutation | CCG,CTG | P634L | NP_006491.2 |
XM_017017759.1 | 1836 | Missense Mutation | CCG,CTG | P613L | XP_016873248.1 |
XM_017017760.1 | 1836 | Missense Mutation | CCG,CTG | P602L | XP_016873249.1 |
XM_017017761.1 | 1836 | Intron | XP_016873250.1 | ||
XM_017017762.1 | 1836 | Intron | XP_016873251.1 |