Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001286341.1 | 239 | Intron | NP_001273270.1 | ||
NM_001286342.1 | 239 | Intron | NP_001273271.1 | ||
NM_152719.2 | 239 | Missense Mutation | CCT,CGT | P51R | NP_689932.1 |
XM_011534971.2 | 239 | Missense Mutation | CCT,CGT | P51R | XP_011533273.1 |