Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_021077.3 | 622 | Missense Mutation | CCA,CTA | P68L | NP_066563.2 |
NM_205858.1 | 622 | Missense Mutation | CCA,CTA | P68L | NP_995580.1 |
XM_017022239.1 | 622 | Intron | XP_016877728.1 |