Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_002250.2 | 1655 | Missense Mutation | CCA,CTA | P420L | NP_002241.1 |
XM_005258882.2 | 1655 | Missense Mutation | CCA,CTA | P388L | XP_005258939.1 |
XM_005258883.2 | 1655 | Missense Mutation | CCA,CTA | P357L | XP_005258940.1 |
XM_011526938.1 | 1655 | Intron | XP_011525240.1 |