Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003635.3 | 3388 | Missense Mutation | CAG,CGG | Q874R | NP_003626.1 |
XM_005270255.3 | 3388 | UTR 3 | XP_005270312.1 | ||
XM_005270256.3 | 3388 | Missense Mutation | CAG,CGG | Q500R | XP_005270313.1 |
XM_011540310.2 | 3388 | Missense Mutation | CAG,CGG | Q874R | XP_011538612.1 |
XM_017016857.1 | 3388 | Missense Mutation | CAG,CGG | Q397R | XP_016872346.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001242487.1 | 3388 | Intron | NP_001229416.1 | ||
NM_001242488.1 | 3388 | Intron | NP_001229417.1 | ||
NM_015037.3 | 3388 | Intron | NP_055852.2 | ||
XM_005269648.2 | 3388 | Intron | XP_005269705.1 | ||
XM_005269653.3 | 3388 | Intron | XP_005269710.1 | ||
XM_005269655.3 | 3388 | Intron | XP_005269712.1 | ||
XM_006717725.3 | 3388 | Intron | XP_006717788.1 | ||
XM_011539544.1 | 3388 | Intron | XP_011537846.1 | ||
XM_017015978.1 | 3388 | Intron | XP_016871467.1 |