Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001127229.1 | 239 | Missense Mutation | CCT,CTT | P22L | NP_001120701.1 |
NM_001127230.1 | 239 | Missense Mutation | CCT,CTT | P22L | NP_001120702.1 |
NM_017900.2 | 239 | Missense Mutation | CCT,CTT | P22L | NP_060370.1 |
XM_011541670.2 | 239 | Missense Mutation | CCT,CTT | P51L | XP_011539972.1 |