ENST00000369409.9:c.387G>A
|
ENSP00000358417.5:p.Lys129=
|
|
ENST00000462324.2:n.470G>A
|
|
|
ENST00000641023.2:c.387G>A
MANE Select
|
ENSP00000493175.1:p.Lys129=
|
|
ENST00000641074.1:c.387G>A
|
ENSP00000493446.1:p.Lys129=
|
|
ENST00000641115.1:c.387G>A
|
ENSP00000493264.1:p.Lys129=
|
|
ENST00000641213.1:c.*40G>A
|
ENSP00000493079.1:n.*40G>A
|
|
ENST00000641247.1:c.*106G>A
|
ENSP00000492955.1:n.*106G>A
|
|
ENST00000641272.1:c.321G>A
|
ENSP00000493432.1:p.Lys107=
|
|
ENST00000641314.1:n.372G>A
|
|
|
ENST00000641371.1:c.301G>A
|
ENSP00000493305.1:p.Gly101Arg
|
|
ENST00000641375.1:c.*223G>A
|
ENSP00000493089.1:n.*223G>A
|
|
ENST00000641491.1:c.*40G>A
|
ENSP00000493187.1:n.*40G>A
|
|
ENST00000641513.1:c.*131G>A
|
ENSP00000493398.1:n.*131G>A
|
|
ENST00000641570.1:c.*106G>A
|
ENSP00000493213.1:n.*106G>A
|
|
ENST00000641573.1:n.475G>A
|
|
|
ENST00000641587.1:c.*98G>A
|
ENSP00000493453.1:n.*98G>A
|
|
ENST00000641597.1:c.387G>A
|
ENSP00000493382.1:p.Lys129=
|
|
ENST00000641711.1:n.611G>A
|
|
|
ENST00000641756.1:c.*131G>A
|
ENSP00000493147.1:n.*131G>A
|
|
ENST00000641811.1:c.143G>A
|
|
|
ENST00000641847.1:n.246G>A
|
|
|
ENST00000641891.1:c.*213G>A
|
ENSP00000493288.1:n.*213G>A
|
|
ENST00000641927.1:n.327G>A
|
|
|
ENST00000641947.1:c.387G>A
|
ENSP00000492994.1:p.Lys129=
|
|
ENST00000642021.1:n.509G>A
|
|
|
ENST00000642041.1:c.*426G>A
|
ENSP00000493415.1:n.*426G>A
|
|
ENST00000369407.3:c.285G>A
|
ENSP00000358415.3:p.Lys95=
|
|
ENST00000369409.8:c.387G>A
|
ENSP00000358417.4:p.Lys129=
|
|
ENST00000462324.1:n.655G>A
|
|
|
ENST00000493622.5:n.576G>A
|
|
|
NM_006623.3:c.387G>A
|
NP_006614.2:p.Lys129=
|
|
XM_011541226.1:c.609G>A
|
XP_011539528.1:p.Lys203=
|
|
XM_011541227.1:c.531G>A
|
XP_011539529.1:p.Lys177=
|
|
XM_011541228.1:c.498G>A
|
XP_011539530.1:p.Lys166=
|
|
XM_011541229.1:c.324G>A
|
XP_011539531.1:p.Lys108=
|
|
XM_011541230.1:c.102G>A
|
XP_011539532.1:p.Lys34=
|
|
XM_011541231.1:c.93G>A
|
XP_011539533.1:p.Lys31=
|
|
XM_011541226.2:c.609G>A
|
XP_011539528.1:p.Lys203=
|
|
XM_011541227.2:c.531G>A
|
XP_011539529.1:p.Lys177=
|
|
XM_011541228.2:c.498G>A
|
XP_011539530.1:p.Lys166=
|
|
XM_011541231.2:c.93G>A
|
XP_011539533.1:p.Lys31=
|
|
XM_024446338.1:c.498G>A
|
XP_024302106.1:p.Lys166=
|
|
NM_006623.4:c.387G>A
MANE Select
|
NP_006614.2:p.Lys129=
|
|