ENST00000369409.9:c.423A>C
|
ENSP00000358417.5:p.Thr141=
|
|
ENST00000462324.2:n.506A>C
|
|
|
ENST00000641023.2:c.423A>C
MANE Select
|
ENSP00000493175.1:p.Thr141=
|
|
ENST00000641074.1:c.423A>C
|
ENSP00000493446.1:p.Thr141=
|
|
ENST00000641115.1:c.423A>C
|
ENSP00000493264.1:p.Thr141=
|
|
ENST00000641213.1:c.*76A>C
|
ENSP00000493079.1:n.*76A>C
|
|
ENST00000641247.1:c.*142A>C
|
ENSP00000492955.1:n.*142A>C
|
|
ENST00000641272.1:c.357A>C
|
ENSP00000493432.1:p.Thr119=
|
|
ENST00000641314.1:n.408A>C
|
|
|
ENST00000641371.1:c.337A>C
|
ENSP00000493305.1:p.Arg113=
|
|
ENST00000641375.1:c.*259A>C
|
ENSP00000493089.1:n.*259A>C
|
|
ENST00000641491.1:c.*76A>C
|
ENSP00000493187.1:n.*76A>C
|
|
ENST00000641570.1:c.*142A>C
|
ENSP00000493213.1:n.*142A>C
|
|
ENST00000641573.1:n.511A>C
|
|
|
ENST00000641587.1:c.*134A>C
|
ENSP00000493453.1:n.*134A>C
|
|
ENST00000641597.1:c.423A>C
|
ENSP00000493382.1:p.Thr141=
|
|
ENST00000641711.1:n.647A>C
|
|
|
ENST00000641756.1:c.*167A>C
|
ENSP00000493147.1:n.*167A>C
|
|
ENST00000641811.1:c.179A>C
|
|
|
ENST00000641847.1:n.282A>C
|
|
|
ENST00000641891.1:c.*249A>C
|
ENSP00000493288.1:n.*249A>C
|
|
ENST00000641927.1:n.363A>C
|
|
|
ENST00000641947.1:c.423A>C
|
ENSP00000492994.1:p.Thr141=
|
|
ENST00000642021.1:n.545A>C
|
|
|
ENST00000642041.1:c.*462A>C
|
ENSP00000493415.1:n.*462A>C
|
|
ENST00000369407.3:c.321A>C
|
ENSP00000358415.3:p.Thr107=
|
|
ENST00000369409.8:c.423A>C
|
ENSP00000358417.4:p.Thr141=
|
|
ENST00000462324.1:n.691A>C
|
|
|
ENST00000493622.5:n.612A>C
|
|
|
NM_006623.3:c.423A>C
|
NP_006614.2:p.Thr141=
|
|
XM_011541226.1:c.645A>C
|
XP_011539528.1:p.Thr215=
|
|
XM_011541227.1:c.567A>C
|
XP_011539529.1:p.Thr189=
|
|
XM_011541228.1:c.534A>C
|
XP_011539530.1:p.Thr178=
|
|
XM_011541229.1:c.360A>C
|
XP_011539531.1:p.Thr120=
|
|
XM_011541230.1:c.138A>C
|
XP_011539532.1:p.Thr46=
|
|
XM_011541231.1:c.129A>C
|
XP_011539533.1:p.Thr43=
|
|
XM_011541226.2:c.645A>C
|
XP_011539528.1:p.Thr215=
|
|
XM_011541227.2:c.567A>C
|
XP_011539529.1:p.Thr189=
|
|
XM_011541228.2:c.534A>C
|
XP_011539530.1:p.Thr178=
|
|
XM_011541231.2:c.129A>C
|
XP_011539533.1:p.Thr43=
|
|
XM_024446338.1:c.534A>C
|
XP_024302106.1:p.Thr178=
|
|
NM_006623.4:c.423A>C
MANE Select
|
NP_006614.2:p.Thr141=
|
|