ENST00000409134.8:c.287G>C
MANE Select
|
ENSP00000387123.3:p.Arg96Thr
|
|
ENST00000412186.2:c.287G>C
|
ENSP00000414536.2:p.Arg96Thr
|
|
ENST00000413020.6:c.287G>C
|
ENSP00000487936.1:p.Arg96Thr
|
|
ENST00000458249.6:c.*196G>C
|
ENSP00000403929.1:n.*196G>C
|
|
ENST00000479989.6:n.470G>C
|
|
|
ENST00000503281.6:c.106+2318G>C
|
|
|
ENST00000509270.2:c.246+662G>C
|
ENSP00000449318.2:n.246+662G>C
|
|
ENST00000509459.6:c.65+2318G>C
|
|
|
ENST00000511266.6:n.1009G>C
|
|
|
ENST00000635851.1:c.285G>C
|
|
|
ENST00000635858.1:n.126G>C
|
|
|
ENST00000635933.1:n.316G>C
|
|
|
ENST00000636062.1:n.182G>C
|
|
|
ENST00000636190.1:n.166G>C
|
|
|
ENST00000636225.1:c.*96G>C
|
ENSP00000490797.1:n.*96G>C
|
|
ENST00000636743.1:c.192+2318G>C
|
ENSP00000489725.1:n.192+2318G>C
|
|
ENST00000636808.1:c.*96G>C
|
ENSP00000490833.1:n.*96G>C
|
|
ENST00000636872.1:c.447G>C
|
ENSP00000490919.1:n.447G>C
|
|
ENST00000636879.1:c.287G>C
|
ENSP00000490811.1:p.Arg96Thr
|
|
ENST00000636886.1:c.192+2318G>C
|
ENSP00000490371.1:n.192+2318G>C
|
|
ENST00000637206.1:c.287G>C
|
ENSP00000489895.1:p.Arg96Thr
|
|
ENST00000637272.1:c.287G>C
|
ENSP00000489686.1:p.Arg96Thr
|
|
ENST00000637782.1:c.287G>C
|
ENSP00000490024.1:p.Arg96Thr
|
|
ENST00000637964.1:c.233G>C
|
ENSP00000490291.1:p.Arg78Thr
|
|
ENST00000638008.1:c.*96G>C
|
ENSP00000490400.1:n.*96G>C
|
|
ENST00000409134.7:c.287G>C
|
ENSP00000387123.3:p.Arg96Thr
|
|
ENST00000412186.1:c.*96G>C
|
ENSP00000414536.1:n.*96G>C
|
|
ENST00000413020.5:c.287G>C
|
ENSP00000487936.1:p.Arg96Thr
|
|
ENST00000447989.6:c.368G>C
|
ENSP00000414132.2:p.Arg123Thr
|
|
ENST00000458249.5:c.447G>C
|
ENSP00000403929.1:n.447G>C
|
|
ENST00000479989.5:n.470G>C
|
|
|
ENST00000503281.5:c.106+2318G>C
|
|
|
ENST00000509270.1:c.192+2318G>C
|
ENSP00000449318.1:n.192+2318G>C
|
|
ENST00000509459.5:c.65+2318G>C
|
|
|
ENST00000510111.6:c.281G>C
|
ENSP00000447388.1:p.Arg94Thr
|
|
ENST00000511266.5:n.242G>C
|
|
|
ENST00000553117.5:c.287G>C
|
ENSP00000448593.1:p.Arg96Thr
|
|
NM_001182.4:c.287G>C
|
NP_001173.2:p.Arg96Thr
|
|
NM_001201377.1:c.203G>C
|
NP_001188306.1:p.Arg68Thr
|
|
NM_001202404.1:c.368G>C
|
NP_001189333.1:p.Arg123Thr
|
|
XM_011543417.1:c.-119G>C
|
XP_011541719.1:n.-119G>C
|
|
XM_011543417.2:c.-119G>C
|
XP_011541719.1:n.-119G>C
|
|
NM_001182.5:c.287G>C
MANE Select
|
NP_001173.2:p.Arg96Thr
|
|
NM_001201377.2:c.203G>C
|
NP_001188306.1:p.Arg68Thr
|
|
NM_001202404.2:c.287G>C
|
NP_001189333.2:p.Arg96Thr
|
|