Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001199138.1 | 3106 | Missense Mutation | AGC,GGC | S988G | NP_001186067.1 |
NM_001199139.1 | 3106 | Missense Mutation | AGC,GGC | S988G | NP_001186068.1 |
NM_001302504.1 | 3106 | Missense Mutation | AGC,GGC | S323G | NP_001289433.1 |
NM_021209.4 | 3106 | Missense Mutation | AGC,GGC | S988G | NP_067032.3 |
XM_017004619.1 | 3106 | Intron | XP_016860108.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
XM_006712048.3 | 3106 | UTR 3 | XP_006712111.1 | ||
XM_011532959.2 | 3106 | UTR 3 | XP_011531261.1 | ||
XM_011532960.2 | 3106 | UTR 3 | XP_011531262.1 | ||
XM_011532961.2 | 3106 | UTR 3 | XP_011531263.1 | ||
XM_011532962.2 | 3106 | UTR 3 | XP_011531264.1 | ||
XM_011532963.2 | 3106 | Intron | XP_011531265.1 | ||
XM_017004462.1 | 3106 | UTR 3 | XP_016859951.1 | ||
XM_017004463.1 | 3106 | Intron | XP_016859952.1 | ||
XM_017004464.1 | 3106 | Intron | XP_016859953.1 | ||
XM_017004465.1 | 3106 | Intron | XP_016859954.1 | ||
XM_017004466.1 | 3106 | Intron | XP_016859955.1 |