ENST00000361740.9:c.857C>G
|
ENSP00000354468.5:p.Ala286Gly
|
|
ENST00000402438.6:c.656C>G
|
ENSP00000385679.1:p.Ala219Gly
|
|
ENST00000407332.6:c.743C>G
|
ENSP00000384457.2:p.Ala248Gly
|
|
ENST00000407623.8:c.656C>G
|
ENSP00000384834.3:p.Ala219Gly
|
|
ENST00000617178.5:c.262C>G
|
|
|
ENST00000684963.1:n.2465C>G
|
|
|
ENST00000685184.1:n.317C>G
|
|
|
ENST00000686523.1:c.*674C>G
|
ENSP00000508940.1:n.*674C>G
|
|
ENST00000687183.1:n.1001C>G
|
|
|
ENST00000687198.1:c.656C>G
|
ENSP00000508492.1:p.Ala219Gly
|
|
ENST00000688117.1:c.824C>G
|
ENSP00000509015.1:p.Ala275Gly
|
|
ENST00000688244.1:c.425C>G
|
ENSP00000510355.1:p.Ala142Gly
|
|
ENST00000689001.1:n.1347C>G
|
|
|
ENST00000689195.1:c.641C>G
|
ENSP00000509895.1:p.Ala214Gly
|
|
ENST00000689239.1:n.892C>G
|
|
|
ENST00000689795.1:n.986C>G
|
|
|
ENST00000690835.1:c.*104C>G
|
ENSP00000509038.1:n.*104C>G
|
|
ENST00000690993.1:n.1480C>G
|
|
|
ENST00000691295.1:c.*208C>G
|
ENSP00000508706.1:n.*208C>G
|
|
ENST00000691918.1:c.1015C>G
|
ENSP00000509525.1:n.1015C>G
|
|
ENST00000692152.1:c.656C>G
|
ENSP00000509317.1:p.Ala219Gly
|
|
ENST00000692344.1:n.1212C>G
|
|
|
ENST00000693363.1:c.767C>G
|
ENSP00000510411.1:p.Ala256Gly
|
|
ENST00000693367.1:c.725C>G
|
ENSP00000508815.1:p.Ala242Gly
|
|
ENST00000693639.1:c.718C>G
|
ENSP00000510223.1:n.718C>G
|
|
ENST00000693646.1:c.631C>G
|
ENSP00000508449.1:n.631C>G
|
|
ENST00000352397.10:c.725C>G
MANE Select
|
ENSP00000338461.6:p.Ala242Gly
|
|
ENST00000352397.9:c.725C>G
|
ENSP00000338461.6:p.Ala242Gly
|
|
ENST00000361740.8:c.824C>G
|
ENSP00000354468.4:p.Ala275Gly
|
|
ENST00000402438.5:c.656C>G
|
ENSP00000385679.1:p.Ala219Gly
|
|
ENST00000407332.5:c.656C>G
|
ENSP00000384457.1:p.Ala219Gly
|
|
ENST00000407623.7:c.656C>G
|
ENSP00000384834.3:p.Ala219Gly
|
|
ENST00000470741.1:n.2859C>G
|
|
|
NM_000398.6:c.725C>G
|
NP_000389.1:p.Ala242Gly
|
|
NM_001129819.2:c.656C>G
|
NP_001123291.1:p.Ala219Gly
|
|
NM_001171660.1:c.824C>G
|
NP_001165131.1:p.Ala275Gly
|
|
NM_001171661.1:c.656C>G
|
NP_001165132.1:p.Ala219Gly
|
|
NM_007326.4:c.656C>G
|
NP_015565.1:p.Ala219Gly
|
|
NM_000398.7:c.725C>G
MANE Select
|
NP_000389.1:p.Ala242Gly
|
|
NM_001171660.2:c.824C>G
|
NP_001165131.1:p.Ala275Gly
|
|