ENST00000288840.10:c.993G>C
MANE Select
|
ENSP00000288840.5:p.Trp331Cys
|
|
ENST00000288840.9:c.993G>C
|
ENSP00000288840.5:p.Trp331Cys
|
|
ENST00000557916.5:c.1125G>C
|
ENSP00000452955.1:n.1125G>C
|
|
ENST00000559931.5:c.297G>C
|
ENSP00000453446.1:n.297G>C
|
|
NM_005585.4:c.993G>C
|
NP_005576.3:p.Trp331Cys
|
|
NR_027654.1:n.2048G>C
|
|
|
XM_011521561.1:c.210G>C
|
XP_011519863.1:p.Trp70Cys
|
|
XR_931825.1:n.2392G>C
|
|
|
XM_011521561.2:c.210G>C
|
XP_011519863.1:p.Trp70Cys
|
|
NM_005585.5:c.993G>C
MANE Select
|
NP_005576.3:p.Trp331Cys
|
|
NR_027654.2:n.2148G>C
|
|
|