Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_178564.3 | 1056 | Missense Mutation | CTC,TTC | L306F | NP_848659.2 |
XM_017013378.1 | 1056 | Missense Mutation | CTC,TTC | L306F | XP_016868867.1 |
XM_017013379.1 | 1056 | Missense Mutation | CTC,TTC | L306F | XP_016868868.1 |
XM_017013380.1 | 1056 | Missense Mutation | CTC,TTC | L306F | XP_016868869.1 |
XM_017013381.1 | 1056 | Missense Mutation | CTC,TTC | L306F | XP_016868870.1 |
XM_017013382.1 | 1056 | Missense Mutation | CTC,TTC | L306F | XP_016868871.1 |
XM_017013383.1 | 1056 | Missense Mutation | CTC,TTC | L306F | XP_016868872.1 |