ENST00000369409.9:c.386A>G
|
ENSP00000358417.5:p.Lys129Arg
|
|
ENST00000462324.2:n.469A>G
|
|
|
ENST00000641023.2:c.386A>G
MANE Select
|
ENSP00000493175.1:p.Lys129Arg
|
|
ENST00000641074.1:c.386A>G
|
ENSP00000493446.1:p.Lys129Arg
|
|
ENST00000641115.1:c.386A>G
|
ENSP00000493264.1:p.Lys129Arg
|
|
ENST00000641213.1:c.*39A>G
|
ENSP00000493079.1:n.*39A>G
|
|
ENST00000641247.1:c.*105A>G
|
ENSP00000492955.1:n.*105A>G
|
|
ENST00000641272.1:c.320A>G
|
ENSP00000493432.1:p.Lys107Arg
|
|
ENST00000641314.1:n.371A>G
|
|
|
ENST00000641371.1:c.300A>G
|
ENSP00000493305.1:p.Glu100=
|
|
ENST00000641375.1:c.*222A>G
|
ENSP00000493089.1:n.*222A>G
|
|
ENST00000641491.1:c.*39A>G
|
ENSP00000493187.1:n.*39A>G
|
|
ENST00000641513.1:c.*130A>G
|
ENSP00000493398.1:n.*130A>G
|
|
ENST00000641570.1:c.*105A>G
|
ENSP00000493213.1:n.*105A>G
|
|
ENST00000641573.1:n.474A>G
|
|
|
ENST00000641587.1:c.*97A>G
|
ENSP00000493453.1:n.*97A>G
|
|
ENST00000641597.1:c.386A>G
|
ENSP00000493382.1:p.Lys129Arg
|
|
ENST00000641711.1:n.610A>G
|
|
|
ENST00000641756.1:c.*130A>G
|
ENSP00000493147.1:n.*130A>G
|
|
ENST00000641811.1:c.142A>G
|
|
|
ENST00000641847.1:n.245A>G
|
|
|
ENST00000641891.1:c.*212A>G
|
ENSP00000493288.1:n.*212A>G
|
|
ENST00000641927.1:n.326A>G
|
|
|
ENST00000641947.1:c.386A>G
|
ENSP00000492994.1:p.Lys129Arg
|
|
ENST00000642021.1:n.508A>G
|
|
|
ENST00000642041.1:c.*425A>G
|
ENSP00000493415.1:n.*425A>G
|
|
ENST00000369407.3:c.284A>G
|
ENSP00000358415.3:p.Lys95Arg
|
|
ENST00000369409.8:c.386A>G
|
ENSP00000358417.4:p.Lys129Arg
|
|
ENST00000462324.1:n.654A>G
|
|
|
ENST00000493622.5:n.575A>G
|
|
|
NM_006623.3:c.386A>G
|
NP_006614.2:p.Lys129Arg
|
|
XM_011541226.1:c.608A>G
|
XP_011539528.1:p.Lys203Arg
|
|
XM_011541227.1:c.530A>G
|
XP_011539529.1:p.Lys177Arg
|
|
XM_011541228.1:c.497A>G
|
XP_011539530.1:p.Lys166Arg
|
|
XM_011541229.1:c.323A>G
|
XP_011539531.1:p.Lys108Arg
|
|
XM_011541230.1:c.101A>G
|
XP_011539532.1:p.Lys34Arg
|
|
XM_011541231.1:c.92A>G
|
XP_011539533.1:p.Lys31Arg
|
|
XM_011541226.2:c.608A>G
|
XP_011539528.1:p.Lys203Arg
|
|
XM_011541227.2:c.530A>G
|
XP_011539529.1:p.Lys177Arg
|
|
XM_011541228.2:c.497A>G
|
XP_011539530.1:p.Lys166Arg
|
|
XM_011541231.2:c.92A>G
|
XP_011539533.1:p.Lys31Arg
|
|
XM_024446338.1:c.497A>G
|
XP_024302106.1:p.Lys166Arg
|
|
NM_006623.4:c.386A>G
MANE Select
|
NP_006614.2:p.Lys129Arg
|
|