|
ENST00000313771.10:n.1117A>G
|
|
|
|
ENST00000355740.8:c.*131A>G
|
ENSP00000347979.3:n.*131A>G
|
|
|
ENST00000357339.7:c.745A>G
|
ENSP00000349896.2:p.Thr249Ala
|
|
|
ENST00000371857.8:n.2353A>G
|
|
|
|
ENST00000460510.6:c.91A>G
|
ENSP00000512812.1:p.Thr31Ala
|
|
|
ENST00000466081.6:n.2457A>G
|
|
|
|
ENST00000477270.6:c.853A>G
|
ENSP00000512813.1:p.Thr285Ala
|
|
|
ENST00000479522.6:c.*237A>G
|
ENSP00000424113.1:n.*237A>G
|
|
|
ENST00000484444.6:c.*249A>G
|
ENSP00000420975.1:n.*249A>G
|
|
|
ENST00000488877.6:c.699A>G
|
ENSP00000425159.1:n.699A>G
|
|
|
ENST00000492756.7:c.*237A>G
|
ENSP00000422453.1:n.*237A>G
|
|
|
ENST00000494799.6:c.91A>G
|
ENSP00000512834.1:p.Thr31Ala
|
|
|
ENST00000562983.3:c.91A>G
|
ENSP00000512845.1:p.Thr31Ala
|
|
|
ENST00000612663.6:c.*210A>G
|
ENSP00000477997.3:n.*210A>G
|
|
|
ENST00000640140.2:n.953A>G
|
|
|
|
ENST00000640250.2:n.307A>G
|
|
|
|
ENST00000640681.2:n.912A>G
|
|
|
|
ENST00000696723.1:n.4441A>G
|
|
|
|
ENST00000696741.1:n.2446A>G
|
|
|
|
ENST00000696742.1:n.2173A>G
|
|
|
|
ENST00000696743.1:n.3576A>G
|
|
|
|
ENST00000696744.1:n.847A>G
|
|
|
|
ENST00000696767.1:n.1142A>G
|
|
|
|
ENST00000696768.1:c.*131A>G
|
ENSP00000512859.1:n.*131A>G
|
|
|
ENST00000696769.1:n.2497A>G
|
|
|
|
ENST00000696771.1:c.91A>G
|
ENSP00000512860.1:p.Thr31Ala
|
|
|
ENST00000696772.1:n.2411A>G
|
|
|
|
ENST00000696773.1:n.2150A>G
|
|
|
|
ENST00000696774.1:n.5918A>G
|
|
|
|
ENST00000696776.1:c.901A>G
|
ENSP00000512861.1:p.Thr301Ala
|
|
|
ENST00000696777.1:n.2216A>G
|
|
|
|
ENST00000696778.1:n.1244A>G
|
|
|
|
ENST00000696779.1:c.415A>G
|
ENSP00000512862.1:p.Thr139Ala
|
|
|
ENST00000696780.1:c.838A>G
|
ENSP00000512863.1:p.Thr280Ala
|
|
|
ENST00000696781.1:c.553A>G
|
ENSP00000512864.1:p.Thr185Ala
|
|
|
ENST00000696782.1:c.*210A>G
|
ENSP00000512865.1:n.*210A>G
|
|
|
ENST00000696783.1:n.2676A>G
|
|
|
|
ENST00000696992.1:n.1925A>G
|
|
|
|
ENST00000696995.1:n.4337A>G
|
|
|
|
ENST00000696996.1:n.2250A>G
|
|
|
|
ENST00000696997.1:c.*438A>G
|
ENSP00000513028.1:n.*438A>G
|
|
|
ENST00000696998.1:n.2062A>G
|
|
|
|
ENST00000696999.1:c.91A>G
|
ENSP00000513029.1:p.Thr31Ala
|
|
|
ENST00000697035.1:c.*141A>G
|
ENSP00000513059.1:n.*141A>G
|
|
|
ENST00000697036.1:c.*224A>G
|
ENSP00000513060.1:n.*224A>G
|
|
|
ENST00000697037.1:n.843A>G
|
|
|
|
ENST00000697093.1:n.3044A>G
|
|
|
|
ENST00000697094.1:n.3391A>G
|
|
|
|
ENST00000697095.1:c.*2009A>G
|
ENSP00000513104.1:n.*2009A>G
|
|
|
ENST00000697096.1:n.1941A>G
|
|
|
|
ENST00000697097.1:c.91A>G
|
ENSP00000513105.1:p.Thr31Ala
|
|
|
ENST00000562983.2:n.994A>G
|
|
|
|
ENST00000690268.1:c.889A>G
|
ENSP00000509810.1:p.Thr297Ala
|
|
|
ENST00000355740.7:c.*134A>G
|
ENSP00000347979.3:n.*134A>G
|
|
|
ENST00000612663.5:c.*210A>G
|
ENSP00000477997.3:n.*210A>G
|
|
|
ENST00000640140.1:n.980A>G
|
|
|
|
ENST00000640250.1:n.307A>G
|
|
|
|
ENST00000640681.1:n.929A>G
|
|
|
|
ENST00000652046.1:c.808A>G
MANE Select
|
ENSP00000498466.1:p.Thr270Ala
|
|
|
ENST00000352159.8:c.*125A>G
|
ENSP00000345601.4:n.*125A>G
|
|
|
ENST00000355279.2:c.783A>G
|
ENSP00000347426.2:n.783A>G
|
|
|
ENST00000355740.6:c.808A>G
|
ENSP00000347979.2:p.Thr270Ala
|
|
|
ENST00000357339.6:c.745A>G
|
ENSP00000349896.2:p.Thr249Ala
|
|
|
ENST00000479522.5:c.*237A>G
|
ENSP00000424113.1:n.*237A>G
|
|
|
ENST00000484444.5:c.*249A>G
|
ENSP00000420975.1:n.*249A>G
|
|
|
ENST00000488877.5:c.*249A>G
|
ENSP00000425159.1:n.*249A>G
|
|
|
ENST00000492756.5:c.636A>G
|
ENSP00000422453.1:n.636A>G
|
|
|
ENST00000494410.5:c.*166A>G
|
ENSP00000423755.1:n.*166A>G
|
|
|
ENST00000612663.4:c.*155A>G
|
ENSP00000477997.2:n.*155A>G
|
|
|
NM_000043.4:c.808A>G , LRG_134t1:c.808A>G
|
NP_000034.1:p.Thr270Ala
|
|
|
NM_152871.2:c.745A>G
|
NP_690610.1:p.Thr249Ala
|
|
|
NM_152872.2:c.*120A>G
|
NP_690611.1:n.*120A>G
|
|
|
NR_028033.2:n.982A>G
|
|
|
|
NR_028034.2:n.844A>G
|
|
|
|
NR_028035.2:n.907A>G
|
|
|
|
NR_028036.2:n.1045A>G
|
|
|
|
XM_006717819.2:c.889A>G
|
XP_006717882.1:p.Thr297Ala
|
|
|
XM_011539764.1:c.970A>G
|
XP_011538066.1:p.Thr324Ala
|
|
|
XM_011539765.1:c.907A>G
|
XP_011538067.1:p.Thr303Ala
|
|
|
XM_011539766.1:c.889A>G
|
XP_011538068.1:p.Thr297Ala
|
|
|
XM_011539767.1:c.853A>G
|
XP_011538069.1:p.Thr285Ala
|
|
|
XR_945732.1:n.876A>G
|
|
|
|
XR_945733.1:n.813A>G
|
|
|
|
NM_000043.5:c.808A>G
|
NP_000034.1:p.Thr270Ala
|
|
|
NM_001320619.1:c.*131A>G
|
NP_001307548.1:n.*131A>G
|
|
|
NM_152871.3:c.745A>G
|
NP_690610.1:p.Thr249Ala
|
|
|
NM_152872.3:c.*120A>G
|
NP_690611.1:n.*120A>G
|
|
|
NR_028033.3:n.954A>G
|
|
|
|
NR_028034.3:n.816A>G
|
|
|
|
NR_028035.3:n.879A>G
|
|
|
|
NR_028036.3:n.1017A>G
|
|
|
|
NR_135313.1:n.934A>G
|
|
|
|
NR_135314.1:n.1117A>G
|
|
|
|
NR_135315.1:n.870A>G
|
|
|
|
XM_006717819.3:c.889A>G
|
XP_006717882.1:p.Thr297Ala
|
|
|
XM_011539764.2:c.970A>G
|
XP_011538066.1:p.Thr324Ala
|
|
|
XM_011539765.2:c.907A>G
|
XP_011538067.1:p.Thr303Ala
|
|
|
XM_011539766.2:c.889A>G
|
XP_011538068.1:p.Thr297Ala
|
|
|
XM_011539767.3:c.853A>G
|
XP_011538069.1:p.Thr285Ala
|
|
|
XR_945732.3:n.876A>G
|
|
|
|
XR_945733.2:n.813A>G
|
|
|
|
NM_000043.6:c.808A>G
MANE Select
|
NP_000034.1:p.Thr270Ala
|
|
|
NM_001320619.2:c.*131A>G
|
NP_001307548.1:n.*131A>G
|
|
|
NM_152871.4:c.745A>G
|
NP_690610.1:p.Thr249Ala
|
|
|
NM_152872.4:c.*120A>G
|
NP_690611.1:n.*120A>G
|
|
|
NR_028033.4:n.715A>G
|
|
|
|
NR_028034.4:n.577A>G
|
|
|
|
NR_028035.4:n.640A>G
|
|
|
|
NR_028036.4:n.778A>G
|
|
|
|
NR_135313.2:n.695A>G
|
|
|
|
NR_135314.2:n.974A>G
|
|
|
|
NR_135315.2:n.727A>G
|
|
|
