Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_052925.3 | 1413 | Intron | NP_443157.1 | ||
XM_005278248.4 | 1413 | Intron | XP_005278305.1 | ||
XM_005278249.4 | 1413 | Intron | XP_005278306.1 | ||
XM_005278250.4 | 1413 | Intron | XP_005278307.1 | ||
XM_005278252.4 | 1413 | Intron | XP_005278309.1 | ||
XM_006722996.3 | 1413 | Intron | XP_006723059.1 | ||
XM_006722997.3 | 1413 | Intron | XP_006723060.1 | ||
XM_011526413.2 | 1413 | Intron | XP_011524715.1 | ||
XM_011526414.2 | 1413 | Intron | XP_011524716.1 | ||
XM_011526415.2 | 1413 | Intron | XP_011524717.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001301782.1 | 1413 | Missense Mutation | ACC,GCC | T409A | NP_001288711.1 |
NM_198988.1 | 1413 | Missense Mutation | ACC,GCC | T432A | NP_945339.2 |