|
NM_001082486.2:c.847G>A
MANE Select
|
NP_001075955.2:p.Gly283Ser
|
|
ENST00000620761.6:c.847G>A
MANE Select
|
ENSP00000478084.1:p.Gly283Ser
|
|
NM_001082486.1:c.1105G>A
|
NP_001075955.1:p.Gly369Ser
|
|
NM_001082487.1:c.1096G>A
|
NP_001075956.1:p.Gly366Ser
|
|
NM_022914.2:c.1096G>A
|
NP_075065.2:p.Gly366Ser
|
|
NM_022914.3:c.838G>A
|
NP_075065.3:p.Gly280Ser
|
|
ENST00000219251.12:c.1096G>A
|
ENSP00000219251.7:p.Gly366Ser
|
|
ENST00000219251.13:c.838G>A
|
ENSP00000219251.8:p.Gly280Ser
|
|
ENST00000393919.8:c.1105G>A
|
ENSP00000377496.4:p.Gly369Ser
|
|
ENST00000602320.1:c.838G>A
|
ENSP00000473679.2:p.Gly280Ser
|
|
ENST00000602382.5:c.371+210G>A
|
|
|
ENST00000602382.6:c.829+210G>A
|
ENSP00000473313.2:n.829+210G>A
|
|
ENST00000602519.2:n.1337G>A
|
|
|
ENST00000602622.5:n.1846G>A
|
|
|
ENST00000602780.2:n.1852G>A
|
|
|
ENST00000602850.5:c.678G>A
|
ENSP00000473595.2:n.678G>A
|
|
ENST00000602850.6:c.*627G>A
|
ENSP00000473595.3:n.*627G>A
|
|
ENST00000602860.5:n.1285G>A
|
|
|
ENST00000602860.6:n.1767G>A
|
|
|
ENST00000620338.4:c.1105G>A
|
ENSP00000483117.1:p.Gly369Ser
|
|
ENST00000620761.4:c.847G>A
|
ENSP00000478084.1:p.Gly283Ser
|
|
ENST00000695641.1:n.1956G>A
|
|
|
ENST00000695648.1:c.829G>A
|
ENSP00000512081.1:p.Gly277Ser
|
|
ENST00000695649.1:n.2048G>A
|
|
|
ENST00000695656.1:n.1675G>A
|
|
|
ENST00000695657.1:n.1165G>A
|
|
|
ENST00000695658.1:c.847G>A
|
ENSP00000512088.1:p.Gly283Ser
|
|
ENST00000695659.1:c.847G>A
|
ENSP00000512089.1:p.Gly283Ser
|
|
ENST00000695660.1:n.1471G>A
|
|
|
ENST00000695661.1:c.*326G>A
|
ENSP00000512090.1:n.*326G>A
|
|
ENST00000695662.1:c.*326G>A
|
ENSP00000512091.1:n.*326G>A
|
|
ENST00000695694.1:c.802G>A
|
ENSP00000512105.1:p.Gly268Ser
|
|
ENST00000695695.1:n.913G>A
|
|
|
ENST00000695696.1:n.1210+210G>A
|
|
|
ENST00000695697.1:c.760G>A
|
ENSP00000512106.1:p.Gly254Ser
|
|
ENST00000695698.1:n.1097G>A
|
|
|
ENST00000695699.1:n.1135G>A
|
|
|
ENST00000695700.1:n.1404G>A
|
|
|
ENST00000695701.1:n.1246G>A
|
|
|
ENST00000695702.1:n.1073G>A
|
|
|
ENST00000695709.1:n.481+210G>A
|
|
|
ENST00000695710.1:n.1481G>A
|
|
|
ENST00000695711.1:c.*155G>A
|
ENSP00000512109.1:n.*155G>A
|
|
ENST00000695712.1:c.*597G>A
|
ENSP00000512110.1:n.*597G>A
|
|
ENST00000695731.1:c.170G>A
|
|
|
ENST00000695732.1:c.646-492G>A
|
ENSP00000512125.1:n.646-492G>A
|
|
ENST00000695733.1:c.743-317G>A
|
ENSP00000512126.1:n.743-317G>A
|
|
ENST00000695734.1:c.847G>A
|
ENSP00000512127.1:p.Gly283Ser
|
|
ENST00000695735.1:n.257G>A
|
|
|
XM_005256115.2:c.1018G>A
|
XP_005256172.1:p.Gly340Ser
|
|
XM_005256115.4:c.1018G>A
|
XP_005256172.1:p.Gly340Ser
|
|
XR_429727.2:n.1458G>A
|
|
|
XR_429727.3:n.1471G>A
|
|
|
XR_429728.2:n.1371G>A
|
|
|
XR_429728.3:n.1388G>A
|
|