|
ENST00000461526.2:c.757T>G
|
ENSP00000513165.1:p.Cys253Gly
|
|
|
ENST00000697178.1:c.*1506T>G
|
ENSP00000513163.1:n.*1506T>G
|
|
|
ENST00000697180.1:c.587T>G
|
|
|
|
ENST00000697241.1:c.514T>G
|
ENSP00000513206.1:p.Cys172Gly
|
|
|
ENST00000389793.7:c.6082T>G
MANE Select
|
ENSP00000374443.2:p.Cys2028Gly
|
|
|
ENST00000389793.6:c.6082T>G
|
ENSP00000374443.2:p.Cys2028Gly
|
|
|
ENST00000389794.7:c.*1506T>G
|
ENSP00000374444.4:n.*1506T>G
|
|
|
ENST00000489585.5:n.6512+121T>G
|
|
|
|
NM_000081.3:c.6082T>G , LRG_143t1:c.6082T>G
|
NP_000072.2:p.Cys2028Gly
|
|
|
NM_001301365.1:c.6082T>G , LRG_143t2:c.6082T>G
|
NP_001288294.1:p.Cys2028Gly
|
|
|
XM_011544031.1:c.6082T>G
|
XP_011542333.1:p.Cys2028Gly
|
|
|
XM_011544032.1:c.6082T>G
|
XP_011542334.1:p.Cys2028Gly
|
|
|
XM_011544033.1:c.6082T>G
|
XP_011542335.1:p.Cys2028Gly
|
|
|
XM_011544034.1:c.5944T>G
|
XP_011542336.1:p.Cys1982Gly
|
|
|
XM_011544035.1:c.6082T>G
|
XP_011542337.1:p.Cys2028Gly
|
|
|
XM_011544036.1:c.3745T>G
|
XP_011542338.1:p.Cys1249Gly
|
|
|
XM_011544037.1:c.6082T>G
|
XP_011542339.1:p.Cys2028Gly
|
|
|
XM_011544038.1:c.6082T>G
|
XP_011542340.1:p.Cys2028Gly
|
|
|
XM_011544039.1:c.6082T>G
|
XP_011542341.1:p.Cys2028Gly
|
|
|
XM_011544040.1:c.5991T>G
|
XP_011542342.1:p.Phe1997Leu
|
|
|
XM_011544033.2:c.6082T>G
|
XP_011542335.1:p.Cys2028Gly
|
|
|
XM_011544035.2:c.6082T>G
|
XP_011542337.1:p.Cys2028Gly
|
|
|
XM_011544036.2:c.3745T>G
|
XP_011542338.1:p.Cys1249Gly
|
|
|
XM_011544037.2:c.6082T>G
|
XP_011542339.1:p.Cys2028Gly
|
|
|
XM_011544039.2:c.6082T>G
|
XP_011542341.1:p.Cys2028Gly
|
|
|
XM_017000150.1:c.6082T>G
|
XP_016855639.1:p.Cys2028Gly
|
|
|
XM_017000151.1:c.5853T>G
|
XP_016855640.1:p.Phe1951Leu
|
|
|
XR_001736946.2:n.6264T>G
|
|
|
|
XR_001736947.1:n.6264T>G
|
|
|
|
XR_001736948.1:n.6264T>G
|
|
|
|
XR_002959252.1:n.6173T>G
|
|
|
|
NM_000081.4:c.6082T>G
MANE Select
|
NP_000072.2:p.Cys2028Gly
|
|
