Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001177660.2 | 4866 | Intron | NP_001171131.1 | ||
NM_004132.4 | 4866 | Intron | NP_004123.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001261463.1 | 4866 | Missense Mutation | GCC,TCC | A1672S | NP_001248392.1 |
NM_001322945.1 | 4866 | Missense Mutation | GCC,TCC | A1636S | NP_001309874.1 |
NM_006175.4 | 4866 | Missense Mutation | GCC,TCC | A1637S | NP_006166.3 |
NM_198060.3 | 4866 | Missense Mutation | GCC,TCC | A1672S | NP_932326.2 |
XM_005269864.2 | 4866 | Missense Mutation | GCC,TCC | A1637S | XP_005269921.1 |
XM_005269865.2 | 4866 | Missense Mutation | GCC,TCC | A1636S | XP_005269922.1 |
XM_005269867.2 | 4866 | Missense Mutation | GCC,TCC | A1568S | XP_005269924.1 |
XM_006717870.2 | 4866 | Missense Mutation | GCC,TCC | A1637S | XP_006717933.1 |
XM_011539832.2 | 4866 | Missense Mutation | GCC,TCC | A1636S | XP_011538134.1 |