Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001258027.1 | 1818 | Intron | NP_001244956.1 | ||
NM_001321308.1 | 1818 | Intron | NP_001308237.1 | ||
NM_173535.2 | 1818 | Missense Mutation | CCT,GCT | P581A | NP_775806.2 |
XM_011532635.2 | 1818 | Missense Mutation | CCT,GCT | P691A | XP_011530937.1 |
XM_011532637.2 | 1818 | Missense Mutation | CCT,GCT | P691A | XP_011530939.1 |
XM_011532638.2 | 1818 | Intron | XP_011530940.1 | ||
XM_011532639.2 | 1818 | Intron | XP_011530941.1 | ||
XM_011532640.2 | 1818 | Intron | XP_011530942.1 | ||
XM_011532641.2 | 1818 | Intron | XP_011530943.1 | ||
XM_011532642.2 | 1818 | Missense Mutation | CCT,GCT | P551A | XP_011530944.1 |
XM_011532643.1 | 1818 | Missense Mutation | CCT,GCT | P520A | XP_011530945.1 |
XM_017003519.1 | 1818 | Missense Mutation | CCT,GCT | P691A | XP_016859008.1 |