Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001173982.1 | 554 | Missense Mutation | CCG,CTG | P19L | NP_001167453.1 |
NM_018413.5 | 554 | Missense Mutation | CCG,CTG | P19L | NP_060883.1 |
XM_017019369.1 | 554 | Intron | XP_016874858.1 |