|
ENST00000313771.10:n.1279A>G
|
|
|
|
ENST00000355740.8:c.*293A>G
|
ENSP00000347979.3:n.*293A>G
|
|
|
ENST00000357339.7:c.907A>G
|
ENSP00000349896.2:p.Asn303Asp
|
|
|
ENST00000371857.8:n.2515A>G
|
|
|
|
ENST00000460510.6:c.253A>G
|
ENSP00000512812.1:p.Asn85Asp
|
|
|
ENST00000466081.6:n.2619A>G
|
|
|
|
ENST00000477270.6:c.1015A>G
|
ENSP00000512813.1:p.Asn339Asp
|
|
|
ENST00000479522.6:c.*399A>G
|
ENSP00000424113.1:n.*399A>G
|
|
|
ENST00000484444.6:c.*411A>G
|
ENSP00000420975.1:n.*411A>G
|
|
|
ENST00000488877.6:c.861A>G
|
ENSP00000425159.1:n.861A>G
|
|
|
ENST00000492756.7:c.*399A>G
|
ENSP00000422453.1:n.*399A>G
|
|
|
ENST00000494799.6:c.253A>G
|
ENSP00000512834.1:p.Asn85Asp
|
|
|
ENST00000562983.3:c.253A>G
|
ENSP00000512845.1:p.Asn85Asp
|
|
|
ENST00000612663.6:c.*372A>G
|
ENSP00000477997.3:n.*372A>G
|
|
|
ENST00000640140.2:n.1115A>G
|
|
|
|
ENST00000640250.2:n.469A>G
|
|
|
|
ENST00000640681.2:n.1074A>G
|
|
|
|
ENST00000696723.1:n.4603A>G
|
|
|
|
ENST00000696741.1:n.2608A>G
|
|
|
|
ENST00000696742.1:n.2335A>G
|
|
|
|
ENST00000696743.1:n.3738A>G
|
|
|
|
ENST00000696744.1:n.1009A>G
|
|
|
|
ENST00000696767.1:n.1304A>G
|
|
|
|
ENST00000696768.1:c.*293A>G
|
ENSP00000512859.1:n.*293A>G
|
|
|
ENST00000696769.1:n.2659A>G
|
|
|
|
ENST00000696771.1:c.253A>G
|
ENSP00000512860.1:p.Asn85Asp
|
|
|
ENST00000696772.1:n.2573A>G
|
|
|
|
ENST00000696773.1:n.2312A>G
|
|
|
|
ENST00000696774.1:n.6080A>G
|
|
|
|
ENST00000696776.1:c.1063A>G
|
ENSP00000512861.1:p.Asn355Asp
|
|
|
ENST00000696777.1:n.2378A>G
|
|
|
|
ENST00000696778.1:n.1406A>G
|
|
|
|
ENST00000696779.1:c.577A>G
|
ENSP00000512862.1:p.Asn193Asp
|
|
|
ENST00000696780.1:c.1000A>G
|
ENSP00000512863.1:p.Asn334Asp
|
|
|
ENST00000696781.1:c.715A>G
|
ENSP00000512864.1:p.Asn239Asp
|
|
|
ENST00000696782.1:c.*372A>G
|
ENSP00000512865.1:n.*372A>G
|
|
|
ENST00000696783.1:n.2838A>G
|
|
|
|
ENST00000696992.1:n.2087A>G
|
|
|
|
ENST00000696995.1:n.4499A>G
|
|
|
|
ENST00000696996.1:n.2412A>G
|
|
|
|
ENST00000696997.1:c.*600A>G
|
ENSP00000513028.1:n.*600A>G
|
|
|
ENST00000696998.1:n.2224A>G
|
|
|
|
ENST00000696999.1:c.253A>G
|
ENSP00000513029.1:p.Asn85Asp
|
|
|
ENST00000697036.1:c.*386A>G
|
ENSP00000513060.1:n.*386A>G
|
|
|
ENST00000697037.1:n.1005A>G
|
|
|
|
ENST00000697093.1:n.3206A>G
|
|
|
|
ENST00000697094.1:n.3553A>G
|
|
|
|
ENST00000697095.1:c.*2171A>G
|
ENSP00000513104.1:n.*2171A>G
|
|
|
ENST00000697096.1:n.2103A>G
|
|
|
|
ENST00000697097.1:c.253A>G
|
ENSP00000513105.1:p.Asn85Asp
|
|
|
ENST00000562983.2:n.1156A>G
|
|
|
|
ENST00000690268.1:c.1051A>G
|
ENSP00000509810.1:p.Asn351Asp
|
|
|
ENST00000355740.7:c.*296A>G
|
ENSP00000347979.3:n.*296A>G
|
|
|
ENST00000612663.5:c.*372A>G
|
ENSP00000477997.3:n.*372A>G
|
|
|
ENST00000640140.1:n.1142A>G
|
|
|
|
ENST00000640250.1:n.469A>G
|
|
|
|
ENST00000640681.1:n.1091A>G
|
|
|
|
ENST00000652046.1:c.970A>G
MANE Select
|
ENSP00000498466.1:p.Asn324Asp
|
|
|
ENST00000352159.8:c.*287A>G
|
ENSP00000345601.4:n.*287A>G
|
|
|
ENST00000355279.2:c.945A>G
|
ENSP00000347426.2:n.945A>G
|
|
|
ENST00000355740.6:c.970A>G
|
ENSP00000347979.2:p.Asn324Asp
|
|
|
ENST00000357339.6:c.907A>G
|
ENSP00000349896.2:p.Asn303Asp
|
|
|
ENST00000479522.5:c.*399A>G
|
ENSP00000424113.1:n.*399A>G
|
|
|
ENST00000484444.5:c.*411A>G
|
ENSP00000420975.1:n.*411A>G
|
|
|
ENST00000488877.5:c.*411A>G
|
ENSP00000425159.1:n.*411A>G
|
|
|
ENST00000492756.5:c.798A>G
|
ENSP00000422453.1:n.798A>G
|
|
|
ENST00000494410.5:c.*328A>G
|
ENSP00000423755.1:n.*328A>G
|
|
|
ENST00000612663.4:c.*317A>G
|
ENSP00000477997.2:n.*317A>G
|
|
|
NM_000043.4:c.970A>G , LRG_134t1:c.970A>G
|
NP_000034.1:p.Asn324Asp
|
|
|
NM_152871.2:c.907A>G
|
NP_690610.1:p.Asn303Asp
|
|
|
NM_152872.2:c.*282A>G
|
NP_690611.1:n.*282A>G
|
|
|
NR_028033.2:n.1144A>G
|
|
|
|
NR_028034.2:n.1006A>G
|
|
|
|
NR_028035.2:n.1069A>G
|
|
|
|
NR_028036.2:n.1207A>G
|
|
|
|
XM_006717819.2:c.1051A>G
|
XP_006717882.1:p.Asn351Asp
|
|
|
XM_011539764.1:c.1132A>G
|
XP_011538066.1:p.Asn378Asp
|
|
|
XM_011539765.1:c.1069A>G
|
XP_011538067.1:p.Asn357Asp
|
|
|
XM_011539766.1:c.1051A>G
|
XP_011538068.1:p.Asn351Asp
|
|
|
XM_011539767.1:c.1015A>G
|
XP_011538069.1:p.Asn339Asp
|
|
|
XR_945733.1:n.975A>G
|
|
|
|
NM_000043.5:c.970A>G
|
NP_000034.1:p.Asn324Asp
|
|
|
NM_001320619.1:c.*293A>G
|
NP_001307548.1:n.*293A>G
|
|
|
NM_152871.3:c.907A>G
|
NP_690610.1:p.Asn303Asp
|
|
|
NM_152872.3:c.*282A>G
|
NP_690611.1:n.*282A>G
|
|
|
NR_028033.3:n.1116A>G
|
|
|
|
NR_028034.3:n.978A>G
|
|
|
|
NR_028035.3:n.1041A>G
|
|
|
|
NR_028036.3:n.1179A>G
|
|
|
|
NR_135313.1:n.1096A>G
|
|
|
|
NR_135314.1:n.1279A>G
|
|
|
|
NR_135315.1:n.1032A>G
|
|
|
|
XM_006717819.3:c.1051A>G
|
XP_006717882.1:p.Asn351Asp
|
|
|
XM_011539764.2:c.1132A>G
|
XP_011538066.1:p.Asn378Asp
|
|
|
XM_011539765.2:c.1069A>G
|
XP_011538067.1:p.Asn357Asp
|
|
|
XM_011539766.2:c.1051A>G
|
XP_011538068.1:p.Asn351Asp
|
|
|
XM_011539767.3:c.1015A>G
|
XP_011538069.1:p.Asn339Asp
|
|
|
XR_945732.3:n.1038A>G
|
|
|
|
XR_945733.2:n.975A>G
|
|
|
|
NM_000043.6:c.970A>G
MANE Select
|
NP_000034.1:p.Asn324Asp
|
|
|
NM_001320619.2:c.*293A>G
|
NP_001307548.1:n.*293A>G
|
|
|
NM_152871.4:c.907A>G
|
NP_690610.1:p.Asn303Asp
|
|
|
NM_152872.4:c.*282A>G
|
NP_690611.1:n.*282A>G
|
|
|
NR_028033.4:n.877A>G
|
|
|
|
NR_028034.4:n.739A>G
|
|
|
|
NR_028035.4:n.802A>G
|
|
|
|
NR_028036.4:n.940A>G
|
|
|
|
NR_135313.2:n.857A>G
|
|
|
|
NR_135314.2:n.1136A>G
|
|
|
|
NR_135315.2:n.889A>G
|
|
|
