Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001243766.1 | 2201 | Missense Mutation | ACA,GCA | T713A | NP_001230695.1 |
NM_001290129.1 | 2201 | UTR 3 | NP_001277058.1 | ||
NM_001290130.1 | 2201 | UTR 3 | NP_001277059.1 | ||
NM_017739.3 | 2201 | UTR 3 | NP_060209.3 | ||
XM_005271010.1 | 2201 | Missense Mutation | ACA,GCA | T683A | XP_005271067.1 |
XM_006710755.1 | 2201 | Missense Mutation | ACA,GCA | T683A | XP_006710818.1 |
XM_006710756.1 | 2201 | Missense Mutation | ACA,GCA | T713A | XP_006710819.1 |
XM_011541760.2 | 2201 | UTR 3 | XP_011540062.1 | ||
XM_017001690.1 | 2201 | UTR 3 | XP_016857179.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005727.3 | 2201 | Intron | NP_005718.2 | ||
XM_011540460.2 | 2201 | Intron | XP_011538762.1 |