Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001184935.1 | 1565 | Missense Mutation | GCG,TCG | A693S | NP_001171864.1 |
NM_004883.2 | 1565 | Missense Mutation | GCG,TCG | A759S | NP_004874.1 |
NM_013981.3 | 1565 | Missense Mutation | GCG,TCG | A753S | NP_053584.1 |
NM_013982.2 | 1565 | Missense Mutation | GCG,TCG | A767S | NP_053585.1 |
NM_013983.2 | 1565 | Missense Mutation | GCG,TCG | A761S | NP_053586.1 |
XM_005268533.3 | 1565 | Missense Mutation | GCG,TCG | A368S | XP_005268590.1 |
XM_006714810.3 | 1565 | Intron | XP_006714873.1 | ||
XM_011537713.2 | 1565 | Intron | XP_011536015.1 | ||
XM_017010064.1 | 1565 | Missense Mutation | GCG,TCG | A379S | XP_016865553.1 |
XM_017010065.1 | 1565 | Missense Mutation | GCG,TCG | A376S | XP_016865554.1 |
XM_017010066.1 | 1565 | Intron | XP_016865555.1 |