Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_012205.2 | 2390 | Silent Mutation | AGC,AGT | S219S | NP_036337.2 |
XM_005264230.3 | 2390 | Nonsense Mutation | CGA,TGA | R171* | XP_005264287.1 |
XM_011532729.2 | 2390 | Silent Mutation | AGC,AGT | S189S | XP_011531031.1 |
XM_011532730.2 | 2390 | Silent Mutation | AGC,AGT | S185S | XP_011531032.1 |
XM_011532731.2 | 2390 | Nonsense Mutation | CGA,TGA | R141* | XP_011531033.1 |
XM_017003717.1 | 2390 | Nonsense Mutation | CGA,TGA | R137* | XP_016859206.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001282755.1 | 2390 | Intron | NP_001269684.1 | ||
NM_001282756.1 | 2390 | Intron | NP_001269685.1 | ||
NM_020744.3 | 2390 | Intron | NP_065795.1 | ||
XM_005264456.2 | 2390 | Intron | XP_005264513.1 | ||
XM_005264458.2 | 2390 | Intron | XP_005264515.1 | ||
XM_005264459.2 | 2390 | Intron | XP_005264516.1 | ||
XM_017004561.1 | 2390 | Intron | XP_016860050.1 | ||
XM_017004562.1 | 2390 | Intron | XP_016860051.1 |