Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
XM_005266596.1 | 1494 | Missense Mutation | CCT,TCT | P327S | XP_005266653.1 |
XM_005266597.1 | 1494 | UTR 3 | XP_005266654.1 | ||
XM_006719896.3 | 1494 | Intron | XP_006719959.1 | ||
XM_011535312.1 | 1494 | Missense Mutation | CCT,TCT | P211S | XP_011533614.1 |
XM_011535313.1 | 1494 | Missense Mutation | CCT,TCT | P211S | XP_011533615.1 |
XM_011535314.1 | 1494 | Missense Mutation | CCT,TCT | P156S | XP_011533616.1 |
XM_017020853.1 | 1494 | Missense Mutation | CCT,TCT | P211S | XP_016876342.1 |
XM_017020854.1 | 1494 | Missense Mutation | CCT,TCT | P211S | XP_016876343.1 |
XM_017020855.1 | 1494 | Missense Mutation | CCT,TCT | P211S | XP_016876344.1 |