Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_012170.3 | 300 | Missense Mutation | CGT,CTT | R92L | NP_036302.1 |
NM_147188.2 | 300 | Missense Mutation | CGT,CTT | R92L | NP_671717.1 |
XM_011521447.2 | 300 | UTR 5 | XP_011519749.1 |