Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_020872.2 | 1738 | Missense Mutation | CCT,TCT | P1011S | NP_065923.1 |
XM_005264757.3 | 1738 | Missense Mutation | CCT,TCT | P1011S | XP_005264814.1 |
XM_011533768.2 | 1738 | Missense Mutation | CCT,TCT | P1011S | XP_011532070.1 |
XM_017006507.1 | 1738 | Missense Mutation | CCT,TCT | P1011S | XP_016861996.1 |
XM_017006508.1 | 1738 | Missense Mutation | CCT,TCT | P953S | XP_016861997.1 |
XM_017006509.1 | 1738 | Missense Mutation | CCT,TCT | P569S | XP_016861998.1 |