ENST00000361740.9:c.724C>A
|
ENSP00000354468.5:p.Pro242Thr
|
|
ENST00000402438.6:c.523C>A
|
ENSP00000385679.1:p.Pro175Thr
|
|
ENST00000407332.6:c.610C>A
|
ENSP00000384457.2:p.Pro204Thr
|
|
ENST00000407623.8:c.523C>A
|
ENSP00000384834.3:p.Pro175Thr
|
|
ENST00000617178.5:c.129C>A
|
|
|
ENST00000684963.1:n.2332C>A
|
|
|
ENST00000686523.1:c.*541C>A
|
ENSP00000508940.1:n.*541C>A
|
|
ENST00000687183.1:n.868C>A
|
|
|
ENST00000687198.1:c.523C>A
|
ENSP00000508492.1:p.Pro175Thr
|
|
ENST00000688117.1:c.691C>A
|
ENSP00000509015.1:p.Pro231Thr
|
|
ENST00000688244.1:c.334-3457C>A
|
ENSP00000510355.1:n.334-3457C>A
|
|
ENST00000689001.1:n.1214C>A
|
|
|
ENST00000689195.1:c.508C>A
|
ENSP00000509895.1:p.Pro170Thr
|
|
ENST00000689239.1:n.759C>A
|
|
|
ENST00000689795.1:n.754C>A
|
|
|
ENST00000690835.1:c.592C>A
|
ENSP00000509038.1:p.Pro198Thr
|
|
ENST00000690993.1:n.1347C>A
|
|
|
ENST00000691295.1:c.*75C>A
|
ENSP00000508706.1:n.*75C>A
|
|
ENST00000691918.1:c.571C>A
|
ENSP00000509525.1:p.Pro191Thr
|
|
ENST00000692152.1:c.523C>A
|
ENSP00000509317.1:p.Pro175Thr
|
|
ENST00000692344.1:n.1079C>A
|
|
|
ENST00000693363.1:c.634C>A
|
ENSP00000510411.1:p.Pro212Thr
|
|
ENST00000693367.1:c.592C>A
|
ENSP00000508815.1:p.Pro198Thr
|
|
ENST00000693639.1:c.585C>A
|
ENSP00000510223.1:n.585C>A
|
|
ENST00000693646.1:c.498C>A
|
ENSP00000508449.1:n.498C>A
|
|
ENST00000352397.10:c.592C>A
MANE Select
|
ENSP00000338461.6:p.Pro198Thr
|
|
ENST00000352397.9:c.592C>A
|
ENSP00000338461.6:p.Pro198Thr
|
|
ENST00000361740.8:c.691C>A
|
ENSP00000354468.4:p.Pro231Thr
|
|
ENST00000402438.5:c.523C>A
|
ENSP00000385679.1:p.Pro175Thr
|
|
ENST00000407332.5:c.523C>A
|
ENSP00000384457.1:p.Pro175Thr
|
|
ENST00000407623.7:c.523C>A
|
ENSP00000384834.3:p.Pro175Thr
|
|
ENST00000470741.1:n.2726C>A
|
|
|
NM_000398.6:c.592C>A
|
NP_000389.1:p.Pro198Thr
|
|
NM_001129819.2:c.523C>A
|
NP_001123291.1:p.Pro175Thr
|
|
NM_001171660.1:c.691C>A
|
NP_001165131.1:p.Pro231Thr
|
|
NM_001171661.1:c.523C>A
|
NP_001165132.1:p.Pro175Thr
|
|
NM_007326.4:c.523C>A
|
NP_015565.1:p.Pro175Thr
|
|
NM_000398.7:c.592C>A
MANE Select
|
NP_000389.1:p.Pro198Thr
|
|
NM_001171660.2:c.691C>A
|
NP_001165131.1:p.Pro231Thr
|
|