Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001317931.1 | 146 | Missense Mutation | CCT,CTT | P50L | NP_001304860.1 |
NM_003116.2 | 146 | Missense Mutation | CCT,CTT | P127L | NP_003107.1 |
XM_005260520.4 | 146 | Missense Mutation | CCT,CTT | P34L | XP_005260577.1 |
XM_011529009.2 | 146 | Missense Mutation | CCT,CTT | P83L | XP_011527311.1 |