ENST00000369409.9:c.395A>C
|
ENSP00000358417.5:p.Lys132Thr
|
|
ENST00000462324.2:n.478A>C
|
|
|
ENST00000641023.2:c.395A>C
MANE Select
|
ENSP00000493175.1:p.Lys132Thr
|
|
ENST00000641074.1:c.395A>C
|
ENSP00000493446.1:p.Lys132Thr
|
|
ENST00000641115.1:c.395A>C
|
ENSP00000493264.1:p.Lys132Thr
|
|
ENST00000641213.1:c.*48A>C
|
ENSP00000493079.1:n.*48A>C
|
|
ENST00000641247.1:c.*114A>C
|
ENSP00000492955.1:n.*114A>C
|
|
ENST00000641272.1:c.329A>C
|
ENSP00000493432.1:p.Lys110Thr
|
|
ENST00000641314.1:n.380A>C
|
|
|
ENST00000641371.1:c.309A>C
|
ENSP00000493305.1:p.Gln103His
|
|
ENST00000641375.1:c.*231A>C
|
ENSP00000493089.1:n.*231A>C
|
|
ENST00000641491.1:c.*48A>C
|
ENSP00000493187.1:n.*48A>C
|
|
ENST00000641513.1:c.*139A>C
|
ENSP00000493398.1:n.*139A>C
|
|
ENST00000641570.1:c.*114A>C
|
ENSP00000493213.1:n.*114A>C
|
|
ENST00000641573.1:n.483A>C
|
|
|
ENST00000641587.1:c.*106A>C
|
ENSP00000493453.1:n.*106A>C
|
|
ENST00000641597.1:c.395A>C
|
ENSP00000493382.1:p.Lys132Thr
|
|
ENST00000641711.1:n.619A>C
|
|
|
ENST00000641756.1:c.*139A>C
|
ENSP00000493147.1:n.*139A>C
|
|
ENST00000641811.1:c.151A>C
|
|
|
ENST00000641847.1:n.254A>C
|
|
|
ENST00000641891.1:c.*221A>C
|
ENSP00000493288.1:n.*221A>C
|
|
ENST00000641927.1:n.335A>C
|
|
|
ENST00000641947.1:c.395A>C
|
ENSP00000492994.1:p.Lys132Thr
|
|
ENST00000642021.1:n.517A>C
|
|
|
ENST00000642041.1:c.*434A>C
|
ENSP00000493415.1:n.*434A>C
|
|
ENST00000369407.3:c.293A>C
|
ENSP00000358415.3:p.Lys98Thr
|
|
ENST00000369409.8:c.395A>C
|
ENSP00000358417.4:p.Lys132Thr
|
|
ENST00000462324.1:n.663A>C
|
|
|
ENST00000493622.5:n.584A>C
|
|
|
NM_006623.3:c.395A>C
|
NP_006614.2:p.Lys132Thr
|
|
XM_011541226.1:c.617A>C
|
XP_011539528.1:p.Lys206Thr
|
|
XM_011541227.1:c.539A>C
|
XP_011539529.1:p.Lys180Thr
|
|
XM_011541228.1:c.506A>C
|
XP_011539530.1:p.Lys169Thr
|
|
XM_011541229.1:c.332A>C
|
XP_011539531.1:p.Lys111Thr
|
|
XM_011541230.1:c.110A>C
|
XP_011539532.1:p.Lys37Thr
|
|
XM_011541231.1:c.101A>C
|
XP_011539533.1:p.Lys34Thr
|
|
XM_011541226.2:c.617A>C
|
XP_011539528.1:p.Lys206Thr
|
|
XM_011541227.2:c.539A>C
|
XP_011539529.1:p.Lys180Thr
|
|
XM_011541228.2:c.506A>C
|
XP_011539530.1:p.Lys169Thr
|
|
XM_011541231.2:c.101A>C
|
XP_011539533.1:p.Lys34Thr
|
|
XM_024446338.1:c.506A>C
|
XP_024302106.1:p.Lys169Thr
|
|
NM_006623.4:c.395A>C
MANE Select
|
NP_006614.2:p.Lys132Thr
|
|