ENST00000525083.6:n.1215A>G
|
|
|
ENST00000532101.6:n.834A>G
|
|
|
ENST00000532125.2:c.729A>G
|
ENSP00000434178.2:p.Thr243=
|
|
ENST00000533839.6:c.86-367A>G
|
ENSP00000509952.1:n.86-367A>G
|
|
ENST00000534011.6:n.1024A>G
|
|
|
ENST00000685484.1:c.732A>G
|
ENSP00000510622.1:p.Thr244=
|
|
ENST00000685601.1:c.732A>G
|
ENSP00000510603.1:p.Thr244=
|
|
ENST00000685765.1:c.732A>G
|
ENSP00000509991.1:p.Thr244=
|
|
ENST00000685844.1:c.*269A>G
|
ENSP00000509820.1:n.*269A>G
|
|
ENST00000685857.1:n.1471A>G
|
|
|
ENST00000686242.1:c.531A>G
|
ENSP00000508950.1:n.531A>G
|
|
ENST00000686888.1:c.*299A>G
|
ENSP00000509619.1:n.*299A>G
|
|
ENST00000687699.1:c.856A>G
|
ENSP00000508878.1:n.856A>G
|
|
ENST00000687786.1:n.2168A>G
|
|
|
ENST00000688100.1:n.1653A>G
|
|
|
ENST00000688588.1:c.732A>G
|
ENSP00000510802.1:p.Thr244=
|
|
ENST00000688927.1:n.2943A>G
|
|
|
ENST00000689283.1:c.*395A>G
|
ENSP00000509050.1:n.*395A>G
|
|
ENST00000689477.1:c.*625A>G
|
ENSP00000508945.1:n.*625A>G
|
|
ENST00000689765.1:c.*225A>G
|
ENSP00000509625.1:n.*225A>G
|
|
ENST00000690512.1:c.*583A>G
|
ENSP00000509793.1:n.*583A>G
|
|
ENST00000692039.1:c.*530A>G
|
ENSP00000508821.1:n.*530A>G
|
|
ENST00000692336.1:c.756A>G
|
ENSP00000508540.1:p.Thr252=
|
|
ENST00000693133.1:n.1212A>G
|
|
|
ENST00000263578.10:c.732A>G
MANE Select
|
ENSP00000263578.5:p.Thr244=
|
|
ENST00000263578.9:c.732A>G
|
ENSP00000263578.5:p.Thr244=
|
|
ENST00000525083.5:n.452A>G
|
|
|
ENST00000525770.5:c.*364A>G
|
ENSP00000434739.1:n.*364A>G
|
|
ENST00000527004.5:c.*76A>G
|
ENSP00000436374.1:n.*76A>G
|
|
ENST00000530642.1:n.1514A>G
|
|
|
ENST00000532101.5:n.955A>G
|
|
|
ENST00000532125.1:c.690A>G
|
ENSP00000434178.1:p.Thr230=
|
|
ENST00000533395.5:n.465A>G
|
|
|
ENST00000533839.5:n.238-367A>G
|
|
|
ENST00000534011.5:n.784A>G
|
|
|
ENST00000534315.5:n.1044A>G
|
|
|
NM_017547.3:c.732A>G
|
NP_060017.1:p.Thr244=
|
|
NR_037647.1:n.678A>G
|
|
|
NR_037648.1:n.918A>G
|
|
|
XM_006718879.2:c.222A>G
|
XP_006718942.1:p.Thr74=
|
|
XM_006718880.2:c.99A>G
|
XP_006718943.1:p.Thr33=
|
|
XM_006718881.2:c.99A>G
|
XP_006718944.1:p.Thr33=
|
|
XM_011542895.1:c.222A>G
|
XP_011541197.1:p.Thr74=
|
|
XM_011542896.1:c.222A>G
|
XP_011541198.1:p.Thr74=
|
|
XM_006718879.3:c.222A>G
|
XP_006718942.1:p.Thr74=
|
|
XM_006718881.3:c.99A>G
|
XP_006718944.1:p.Thr33=
|
|
XM_011542895.2:c.222A>G
|
XP_011541197.1:p.Thr74=
|
|
XM_011542896.2:c.222A>G
|
XP_011541198.1:p.Thr74=
|
|
XM_017018000.2:c.732A>G
|
XP_016873489.1:p.Thr244=
|
|
XM_017018001.1:c.222A>G
|
XP_016873490.1:p.Thr74=
|
|
XM_017018002.1:c.222A>G
|
XP_016873491.1:p.Thr74=
|
|
XM_017018003.2:c.99A>G
|
XP_016873492.1:p.Thr33=
|
|
XM_017018004.1:c.99A>G
|
XP_016873493.1:p.Thr33=
|
|
XM_017018005.1:c.99A>G
|
XP_016873494.1:p.Thr33=
|
|
XM_017018006.2:c.99A>G
|
XP_016873495.1:p.Thr33=
|
|
NM_017547.4:c.732A>G
MANE Select
|
NP_060017.1:p.Thr244=
|
|
NR_037647.2:n.564A>G
|
|
|
NR_037648.2:n.909A>G
|
|
|