Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001001710.2 | 402 | Intron | NP_001001710.1 | ||
XM_006717108.2 | 402 | Intron | XP_006717171.2 | ||
XM_011518694.1 | 402 | Intron | XP_011516996.1 | ||
XM_011518695.1 | 402 | Intron | XP_011516997.1 | ||
XM_011518696.2 | 402 | Intron | XP_011516998.1 | ||
XM_011518697.1 | 402 | Intron | XP_011516999.1 | ||
XM_017014718.1 | 402 | Intron | XP_016870207.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001004353.3 | 402 | Missense Mutation | AGC,GGC | S126G | NP_001004353.2 |
NM_001256699.1 | 402 | Missense Mutation | AGC,GGC | S126G | NP_001243628.1 |
NM_001256700.1 | 402 | Missense Mutation | AGC,GGC | S126G | NP_001243629.1 |
NM_001256701.1 | 402 | Missense Mutation | AGC,GGC | S126G | NP_001243630.1 |
XM_006717113.2 | 402 | Missense Mutation | AGC,GGC | S126G | XP_006717176.1 |
XM_006717115.2 | 402 | Missense Mutation | AGC,GGC | S126G | XP_006717178.1 |