Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001114377.1 | 1300 | Missense Mutation | TGT,TTT | C336F | NP_001107849.1 |
NM_014009.3 | 1300 | Missense Mutation | TGT,TTT | C371F | NP_054728.2 |
XM_006724533.2 | 1300 | Missense Mutation | TGT,TTT | C394F | XP_006724596.2 |
XM_011543916.2 | 1300 | Missense Mutation | TGT,TTT | C444F | XP_011542218.1 |
XM_017029565.1 | 1300 | Missense Mutation | TGT,TTT | C456F | XP_016885054.1 |
XM_017029566.1 | 1300 | Missense Mutation | TGT,TTT | C444F | XP_016885055.1 |
XM_017029567.1 | 1300 | Missense Mutation | TGT,TTT | C353F | XP_016885056.1 |