Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001243650.1 | 1177 | Intron | NP_001230579.1 | ||
NM_030819.3 | 1177 | Missense Mutation | CCT,CTT | P380L | NP_110446.3 |
XM_006721288.3 | 1177 | Missense Mutation | CCT,CTT | P275L | XP_006721351.1 |
XM_017023738.1 | 1177 | Missense Mutation | CCT,CTT | P380L | XP_016879227.1 |