Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_058004.3 | 130 | Intron | NP_477352.3 | ||
XM_005261634.1 | 130 | Intron | XP_005261691.1 | ||
XM_005261635.1 | 130 | Intron | XP_005261692.1 | ||
XM_011530226.1 | 130 | Intron | XP_011528528.1 | ||
XM_011530228.2 | 130 | Intron | XP_011528530.1 | ||
XM_017028829.1 | 130 | Intron | XP_016884318.1 | ||
XM_017028830.1 | 130 | Intron | XP_016884319.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000185.3 | 130 | Missense Mutation | AGC,AGG | S21R | NP_000176.2 |