ENST00000361740.9:c.856G>T
|
ENSP00000354468.5:p.Ala286Ser
|
|
ENST00000402438.6:c.655G>T
|
ENSP00000385679.1:p.Ala219Ser
|
|
ENST00000407332.6:c.742G>T
|
ENSP00000384457.2:p.Ala248Ser
|
|
ENST00000407623.8:c.655G>T
|
ENSP00000384834.3:p.Ala219Ser
|
|
ENST00000617178.5:c.261G>T
|
|
|
ENST00000684963.1:n.2464G>T
|
|
|
ENST00000685184.1:n.316G>T
|
|
|
ENST00000686523.1:c.*673G>T
|
ENSP00000508940.1:n.*673G>T
|
|
ENST00000687183.1:n.1000G>T
|
|
|
ENST00000687198.1:c.655G>T
|
ENSP00000508492.1:p.Ala219Ser
|
|
ENST00000688117.1:c.823G>T
|
ENSP00000509015.1:p.Ala275Ser
|
|
ENST00000688244.1:c.424G>T
|
ENSP00000510355.1:p.Ala142Ser
|
|
ENST00000689001.1:n.1346G>T
|
|
|
ENST00000689195.1:c.640G>T
|
ENSP00000509895.1:p.Ala214Ser
|
|
ENST00000689239.1:n.891G>T
|
|
|
ENST00000689795.1:n.985G>T
|
|
|
ENST00000690835.1:c.*103G>T
|
ENSP00000509038.1:n.*103G>T
|
|
ENST00000690993.1:n.1479G>T
|
|
|
ENST00000691295.1:c.*207G>T
|
ENSP00000508706.1:n.*207G>T
|
|
ENST00000691918.1:c.1014G>T
|
ENSP00000509525.1:n.1014G>T
|
|
ENST00000692152.1:c.655G>T
|
ENSP00000509317.1:p.Ala219Ser
|
|
ENST00000692344.1:n.1211G>T
|
|
|
ENST00000693363.1:c.766G>T
|
ENSP00000510411.1:p.Ala256Ser
|
|
ENST00000693367.1:c.724G>T
|
ENSP00000508815.1:p.Ala242Ser
|
|
ENST00000693639.1:c.717G>T
|
ENSP00000510223.1:n.717G>T
|
|
ENST00000693646.1:c.630G>T
|
ENSP00000508449.1:n.630G>T
|
|
ENST00000352397.10:c.724G>T
MANE Select
|
ENSP00000338461.6:p.Ala242Ser
|
|
ENST00000352397.9:c.724G>T
|
ENSP00000338461.6:p.Ala242Ser
|
|
ENST00000361740.8:c.823G>T
|
ENSP00000354468.4:p.Ala275Ser
|
|
ENST00000402438.5:c.655G>T
|
ENSP00000385679.1:p.Ala219Ser
|
|
ENST00000407332.5:c.655G>T
|
ENSP00000384457.1:p.Ala219Ser
|
|
ENST00000407623.7:c.655G>T
|
ENSP00000384834.3:p.Ala219Ser
|
|
ENST00000470741.1:n.2858G>T
|
|
|
NM_000398.6:c.724G>T
|
NP_000389.1:p.Ala242Ser
|
|
NM_001129819.2:c.655G>T
|
NP_001123291.1:p.Ala219Ser
|
|
NM_001171660.1:c.823G>T
|
NP_001165131.1:p.Ala275Ser
|
|
NM_001171661.1:c.655G>T
|
NP_001165132.1:p.Ala219Ser
|
|
NM_007326.4:c.655G>T
|
NP_015565.1:p.Ala219Ser
|
|
NM_000398.7:c.724G>T
MANE Select
|
NP_000389.1:p.Ala242Ser
|
|
NM_001171660.2:c.823G>T
|
NP_001165131.1:p.Ala275Ser
|
|