ENST00000369409.9:c.369G>A
|
ENSP00000358417.5:p.Gln123=
|
|
ENST00000462324.2:n.452G>A
|
|
|
ENST00000641023.2:c.369G>A
MANE Select
|
ENSP00000493175.1:p.Gln123=
|
|
ENST00000641074.1:c.369G>A
|
ENSP00000493446.1:p.Gln123=
|
|
ENST00000641115.1:c.369G>A
|
ENSP00000493264.1:p.Gln123=
|
|
ENST00000641213.1:c.*22G>A
|
ENSP00000493079.1:n.*22G>A
|
|
ENST00000641247.1:c.*88G>A
|
ENSP00000492955.1:n.*88G>A
|
|
ENST00000641272.1:c.303G>A
|
ENSP00000493432.1:p.Gln101=
|
|
ENST00000641314.1:n.354G>A
|
|
|
ENST00000641371.1:c.283G>A
|
ENSP00000493305.1:p.Gly95Ser
|
|
ENST00000641375.1:c.*205G>A
|
ENSP00000493089.1:n.*205G>A
|
|
ENST00000641491.1:c.*22G>A
|
ENSP00000493187.1:n.*22G>A
|
|
ENST00000641513.1:c.*113G>A
|
ENSP00000493398.1:n.*113G>A
|
|
ENST00000641570.1:c.*88G>A
|
ENSP00000493213.1:n.*88G>A
|
|
ENST00000641573.1:n.457G>A
|
|
|
ENST00000641587.1:c.*80G>A
|
ENSP00000493453.1:n.*80G>A
|
|
ENST00000641597.1:c.369G>A
|
ENSP00000493382.1:p.Gln123=
|
|
ENST00000641711.1:n.593G>A
|
|
|
ENST00000641756.1:c.*113G>A
|
ENSP00000493147.1:n.*113G>A
|
|
ENST00000641811.1:c.125G>A
|
|
|
ENST00000641847.1:n.228G>A
|
|
|
ENST00000641891.1:c.*195G>A
|
ENSP00000493288.1:n.*195G>A
|
|
ENST00000641927.1:n.309G>A
|
|
|
ENST00000641947.1:c.369G>A
|
ENSP00000492994.1:p.Gln123=
|
|
ENST00000642021.1:n.491G>A
|
|
|
ENST00000642041.1:c.*408G>A
|
ENSP00000493415.1:n.*408G>A
|
|
ENST00000369407.3:c.267G>A
|
ENSP00000358415.3:p.Gln89=
|
|
ENST00000369409.8:c.369G>A
|
ENSP00000358417.4:p.Gln123=
|
|
ENST00000462324.1:n.637G>A
|
|
|
ENST00000493622.5:n.558G>A
|
|
|
NM_006623.3:c.369G>A
|
NP_006614.2:p.Gln123=
|
|
XM_011541226.1:c.591G>A
|
XP_011539528.1:p.Gln197=
|
|
XM_011541227.1:c.513G>A
|
XP_011539529.1:p.Gln171=
|
|
XM_011541228.1:c.480G>A
|
XP_011539530.1:p.Gln160=
|
|
XM_011541229.1:c.306G>A
|
XP_011539531.1:p.Gln102=
|
|
XM_011541230.1:c.84G>A
|
XP_011539532.1:p.Gln28=
|
|
XM_011541231.1:c.75G>A
|
XP_011539533.1:p.Gln25=
|
|
XM_011541226.2:c.591G>A
|
XP_011539528.1:p.Gln197=
|
|
XM_011541227.2:c.513G>A
|
XP_011539529.1:p.Gln171=
|
|
XM_011541228.2:c.480G>A
|
XP_011539530.1:p.Gln160=
|
|
XM_011541231.2:c.75G>A
|
XP_011539533.1:p.Gln25=
|
|
XM_024446338.1:c.480G>A
|
XP_024302106.1:p.Gln160=
|
|
NM_006623.4:c.369G>A
MANE Select
|
NP_006614.2:p.Gln123=
|
|