ENST00000559386.2:c.468A>T
|
ENSP00000452777.2:p.Thr156=
|
|
ENST00000560044.6:c.*463A>T
|
ENSP00000452942.1:n.*463A>T
|
|
ENST00000560595.6:c.468A>T
|
ENSP00000453345.2:p.Thr156=
|
|
ENST00000565910.6:c.468A>T
|
ENSP00000458001.2:p.Thr156=
|
|
ENST00000685118.1:c.*463A>T
|
ENSP00000509473.1:n.*463A>T
|
|
ENST00000685548.1:c.468A>T
|
ENSP00000510343.1:p.Thr156=
|
|
ENST00000685863.1:c.321A>T
|
ENSP00000509361.1:p.Thr107=
|
|
ENST00000687293.1:c.468A>T
|
ENSP00000509928.1:p.Thr156=
|
|
ENST00000687975.1:c.*344A>T
|
ENSP00000508690.1:n.*344A>T
|
|
ENST00000688154.1:c.468A>T
|
ENSP00000510637.1:p.Thr156=
|
|
ENST00000688389.1:c.468A>T
|
ENSP00000510491.1:p.Thr156=
|
|
ENST00000688637.1:n.549A>T
|
|
|
ENST00000688908.1:c.305-2A>T
|
ENSP00000510242.1:n.305-2A>T
|
|
ENST00000689120.1:n.552A>T
|
|
|
ENST00000689730.1:c.452-2A>T
|
ENSP00000510006.1:n.452-2A>T
|
|
ENST00000689739.1:n.549A>T
|
|
|
ENST00000690610.1:c.468A>T
|
ENSP00000510473.1:p.Thr156=
|
|
ENST00000691021.1:c.*463A>T
|
ENSP00000510805.1:n.*463A>T
|
|
ENST00000691071.1:n.247A>T
|
|
|
ENST00000691695.1:c.321A>T
|
ENSP00000509402.1:p.Thr107=
|
|
ENST00000692691.1:c.468A>T
|
ENSP00000508808.1:p.Thr156=
|
|
ENST00000693064.1:c.*443A>T
|
ENSP00000510720.1:n.*443A>T
|
|
ENST00000557943.6:c.468A>T
MANE Select
|
ENSP00000452762.1:p.Thr156=
|
|
ENST00000267950.12:c.*191A>T
|
ENSP00000267950.8:n.*191A>T
|
|
ENST00000433983.6:c.321A>T
|
ENSP00000399273.2:p.Thr107=
|
|
ENST00000557943.5:c.468A>T
|
ENSP00000452762.1:p.Thr156=
|
|
ENST00000559075.5:n.492A>T
|
|
|
ENST00000559386.1:c.468A>T
|
ENSP00000452777.1:p.Thr156=
|
|
ENST00000559602.5:c.156A>T
|
ENSP00000452659.1:p.Thr52=
|
|
ENST00000559758.5:n.309A>T
|
|
|
ENST00000559973.5:c.178A>T
|
|
|
ENST00000560044.5:c.*463A>T
|
ENSP00000452942.1:n.*463A>T
|
|
ENST00000560309.5:c.*381A>T
|
ENSP00000453753.1:n.*381A>T
|
|
ENST00000560345.5:c.280A>T
|
|
|
ENST00000560595.5:c.468A>T
|
ENSP00000453345.1:p.Thr156=
|
|
ENST00000560726.5:c.-313A>T
|
ENSP00000453098.1:n.-313A>T
|
|
ENST00000560816.5:n.27A>T
|
|
|
ENST00000560899.5:c.-313A>T
|
ENSP00000453422.1:n.-313A>T
|
|
NM_000126.3:c.468A>T
|
NP_000117.1:p.Thr156=
|
|
NM_001127716.1:c.321A>T
|
NP_001121188.1:p.Thr107=
|
|
XR_931766.1:n.523A>T
|
|
|
XR_931766.3:n.549A>T
|
|
|
NM_000126.4:c.468A>T
MANE Select
|
NP_000117.1:p.Thr156=
|
|
NM_001127716.2:c.321A>T
|
NP_001121188.1:p.Thr107=
|
|