Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001301140.1 | 1296 | Missense Mutation | CCT,TCT | P46S | NP_001288069.1 |
NM_001301141.1 | 1296 | Missense Mutation | CCT,TCT | P46S | NP_001288070.1 |
NM_001320042.1 | 1296 | Missense Mutation | CCT,TCT | P46S | NP_001306971.1 |
NM_014301.4 | 1296 | Missense Mutation | CCT,TCT | P21S | NP_055116.1 |
NM_213595.3 | 1296 | Missense Mutation | CCT,TCT | P46S | NP_998760.1 |
XM_011538100.2 | 1296 | Missense Mutation | CCT,TCT | P21S | XP_011536402.1 |
XM_011538101.2 | 1296 | Missense Mutation | CCT,TCT | P46S | XP_011536403.1 |