ENST00000361740.9:c.797T>A
|
ENSP00000354468.5:p.Leu266Gln
|
|
ENST00000402438.6:c.596T>A
|
ENSP00000385679.1:p.Leu199Gln
|
|
ENST00000407332.6:c.683T>A
|
ENSP00000384457.2:p.Leu228Gln
|
|
ENST00000407623.8:c.596T>A
|
ENSP00000384834.3:p.Leu199Gln
|
|
ENST00000617178.5:c.202T>A
|
|
|
ENST00000684963.1:n.2405T>A
|
|
|
ENST00000685184.1:n.257T>A
|
|
|
ENST00000686523.1:c.*614T>A
|
ENSP00000508940.1:n.*614T>A
|
|
ENST00000687183.1:n.941T>A
|
|
|
ENST00000687198.1:c.596T>A
|
ENSP00000508492.1:p.Leu199Gln
|
|
ENST00000688117.1:c.764T>A
|
ENSP00000509015.1:p.Leu255Gln
|
|
ENST00000688244.1:c.365T>A
|
ENSP00000510355.1:p.Leu122Gln
|
|
ENST00000689001.1:n.1287T>A
|
|
|
ENST00000689195.1:c.581T>A
|
ENSP00000509895.1:p.Leu194Gln
|
|
ENST00000689239.1:n.832T>A
|
|
|
ENST00000689795.1:n.926T>A
|
|
|
ENST00000690835.1:c.*44T>A
|
ENSP00000509038.1:n.*44T>A
|
|
ENST00000690993.1:n.1420T>A
|
|
|
ENST00000691295.1:c.*148T>A
|
ENSP00000508706.1:n.*148T>A
|
|
ENST00000691918.1:c.955T>A
|
ENSP00000509525.1:n.955T>A
|
|
ENST00000692152.1:c.596T>A
|
ENSP00000509317.1:p.Leu199Gln
|
|
ENST00000692344.1:n.1152T>A
|
|
|
ENST00000693363.1:c.707T>A
|
ENSP00000510411.1:p.Leu236Gln
|
|
ENST00000693367.1:c.665T>A
|
ENSP00000508815.1:p.Leu222Gln
|
|
ENST00000693639.1:c.658T>A
|
ENSP00000510223.1:n.658T>A
|
|
ENST00000693646.1:c.571T>A
|
ENSP00000508449.1:n.571T>A
|
|
ENST00000352397.10:c.665T>A
MANE Select
|
ENSP00000338461.6:p.Leu222Gln
|
|
ENST00000352397.9:c.665T>A
|
ENSP00000338461.6:p.Leu222Gln
|
|
ENST00000361740.8:c.764T>A
|
ENSP00000354468.4:p.Leu255Gln
|
|
ENST00000402438.5:c.596T>A
|
ENSP00000385679.1:p.Leu199Gln
|
|
ENST00000407332.5:c.596T>A
|
ENSP00000384457.1:p.Leu199Gln
|
|
ENST00000407623.7:c.596T>A
|
ENSP00000384834.3:p.Leu199Gln
|
|
ENST00000470741.1:n.2799T>A
|
|
|
NM_000398.6:c.665T>A
|
NP_000389.1:p.Leu222Gln
|
|
NM_001129819.2:c.596T>A
|
NP_001123291.1:p.Leu199Gln
|
|
NM_001171660.1:c.764T>A
|
NP_001165131.1:p.Leu255Gln
|
|
NM_001171661.1:c.596T>A
|
NP_001165132.1:p.Leu199Gln
|
|
NM_007326.4:c.596T>A
|
NP_015565.1:p.Leu199Gln
|
|
NM_000398.7:c.665T>A
MANE Select
|
NP_000389.1:p.Leu222Gln
|
|
NM_001171660.2:c.764T>A
|
NP_001165131.1:p.Leu255Gln
|
|