Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001110798.1 | 413 | Missense Mutation | TCG,TTG | S38L | NP_001104268.1 |
NM_018527.3 | 413 | Missense Mutation | TCG,TTG | S38L | NP_060997.2 |
NM_024561.4 | 413 | Missense Mutation | TCG,TTG | S38L | NP_078837.3 |
XM_005266523.2 | 413 | Intron | XP_005266580.1 | ||
XM_006719866.2 | 413 | Missense Mutation | TCG,TTG | S38L | XP_006719929.1 |
XM_011535227.2 | 413 | Missense Mutation | TCG,TTG | S38L | XP_011533529.1 |
XM_011535228.1 | 413 | Missense Mutation | TCG,TTG | S38L | XP_011533530.1 |
XM_017020744.1 | 413 | Intron | XP_016876233.1 | ||
XM_017020745.1 | 413 | Missense Mutation | TCG,TTG | S38L | XP_016876234.1 |
XM_017020746.1 | 413 | Missense Mutation | TCG,TTG | S38L | XP_016876235.1 |