Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001243738.1 | 2650 | Missense Mutation | CCC,GCC | P681A | NP_001230667.1 |
NM_004761.4 | 2650 | Missense Mutation | CCC,GCC | P763A | NP_004752.1 |
XM_011514781.1 | 2650 | Missense Mutation | CCC,GCC | P656A | XP_011513083.1 |
XM_011514785.2 | 2650 | Intron | XP_011513087.1 |