|
ENST00000313771.10:n.1115A>G
|
|
|
|
ENST00000355740.8:c.*129A>G
|
ENSP00000347979.3:n.*129A>G
|
|
|
ENST00000357339.7:c.743A>G
|
ENSP00000349896.2:p.Asp248Gly
|
|
|
ENST00000371857.8:n.2351A>G
|
|
|
|
ENST00000460510.6:c.89A>G
|
ENSP00000512812.1:p.Asp30Gly
|
|
|
ENST00000466081.6:n.2455A>G
|
|
|
|
ENST00000477270.6:c.851A>G
|
ENSP00000512813.1:p.Asp284Gly
|
|
|
ENST00000479522.6:c.*235A>G
|
ENSP00000424113.1:n.*235A>G
|
|
|
ENST00000484444.6:c.*247A>G
|
ENSP00000420975.1:n.*247A>G
|
|
|
ENST00000488877.6:c.697A>G
|
ENSP00000425159.1:n.697A>G
|
|
|
ENST00000492756.7:c.*235A>G
|
ENSP00000422453.1:n.*235A>G
|
|
|
ENST00000494799.6:c.89A>G
|
ENSP00000512834.1:p.Asp30Gly
|
|
|
ENST00000562983.3:c.89A>G
|
ENSP00000512845.1:p.Asp30Gly
|
|
|
ENST00000612663.6:c.*208A>G
|
ENSP00000477997.3:n.*208A>G
|
|
|
ENST00000640140.2:n.951A>G
|
|
|
|
ENST00000640250.2:n.305A>G
|
|
|
|
ENST00000640681.2:n.910A>G
|
|
|
|
ENST00000696723.1:n.4439A>G
|
|
|
|
ENST00000696741.1:n.2444A>G
|
|
|
|
ENST00000696742.1:n.2171A>G
|
|
|
|
ENST00000696743.1:n.3574A>G
|
|
|
|
ENST00000696744.1:n.845A>G
|
|
|
|
ENST00000696767.1:n.1140A>G
|
|
|
|
ENST00000696768.1:c.*129A>G
|
ENSP00000512859.1:n.*129A>G
|
|
|
ENST00000696769.1:n.2495A>G
|
|
|
|
ENST00000696771.1:c.89A>G
|
ENSP00000512860.1:p.Asp30Gly
|
|
|
ENST00000696772.1:n.2409A>G
|
|
|
|
ENST00000696773.1:n.2148A>G
|
|
|
|
ENST00000696774.1:n.5916A>G
|
|
|
|
ENST00000696776.1:c.899A>G
|
ENSP00000512861.1:p.Asp300Gly
|
|
|
ENST00000696777.1:n.2214A>G
|
|
|
|
ENST00000696778.1:n.1242A>G
|
|
|
|
ENST00000696779.1:c.413A>G
|
ENSP00000512862.1:p.Asp138Gly
|
|
|
ENST00000696780.1:c.836A>G
|
ENSP00000512863.1:p.Asp279Gly
|
|
|
ENST00000696781.1:c.551A>G
|
ENSP00000512864.1:p.Asp184Gly
|
|
|
ENST00000696782.1:c.*208A>G
|
ENSP00000512865.1:n.*208A>G
|
|
|
ENST00000696783.1:n.2674A>G
|
|
|
|
ENST00000696992.1:n.1923A>G
|
|
|
|
ENST00000696995.1:n.4335A>G
|
|
|
|
ENST00000696996.1:n.2248A>G
|
|
|
|
ENST00000696997.1:c.*436A>G
|
ENSP00000513028.1:n.*436A>G
|
|
|
ENST00000696998.1:n.2060A>G
|
|
|
|
ENST00000696999.1:c.89A>G
|
ENSP00000513029.1:p.Asp30Gly
|
|
|
ENST00000697035.1:c.*139A>G
|
ENSP00000513059.1:n.*139A>G
|
|
|
ENST00000697036.1:c.*222A>G
|
ENSP00000513060.1:n.*222A>G
|
|
|
ENST00000697037.1:n.841A>G
|
|
|
|
ENST00000697093.1:n.3042A>G
|
|
|
|
ENST00000697094.1:n.3389A>G
|
|
|
|
ENST00000697095.1:c.*2007A>G
|
ENSP00000513104.1:n.*2007A>G
|
|
|
ENST00000697096.1:n.1939A>G
|
|
|
|
ENST00000697097.1:c.89A>G
|
ENSP00000513105.1:p.Asp30Gly
|
|
|
ENST00000562983.2:n.992A>G
|
|
|
|
ENST00000690268.1:c.887A>G
|
ENSP00000509810.1:p.Asp296Gly
|
|
|
ENST00000355740.7:c.*132A>G
|
ENSP00000347979.3:n.*132A>G
|
|
|
ENST00000612663.5:c.*208A>G
|
ENSP00000477997.3:n.*208A>G
|
|
|
ENST00000640140.1:n.978A>G
|
|
|
|
ENST00000640250.1:n.305A>G
|
|
|
|
ENST00000640681.1:n.927A>G
|
|
|
|
ENST00000652046.1:c.806A>G
MANE Select
|
ENSP00000498466.1:p.Asp269Gly
|
|
|
ENST00000352159.8:c.*123A>G
|
ENSP00000345601.4:n.*123A>G
|
|
|
ENST00000355279.2:c.781A>G
|
ENSP00000347426.2:n.781A>G
|
|
|
ENST00000355740.6:c.806A>G
|
ENSP00000347979.2:p.Asp269Gly
|
|
|
ENST00000357339.6:c.743A>G
|
ENSP00000349896.2:p.Asp248Gly
|
|
|
ENST00000479522.5:c.*235A>G
|
ENSP00000424113.1:n.*235A>G
|
|
|
ENST00000484444.5:c.*247A>G
|
ENSP00000420975.1:n.*247A>G
|
|
|
ENST00000488877.5:c.*247A>G
|
ENSP00000425159.1:n.*247A>G
|
|
|
ENST00000492756.5:c.634A>G
|
ENSP00000422453.1:n.634A>G
|
|
|
ENST00000494410.5:c.*164A>G
|
ENSP00000423755.1:n.*164A>G
|
|
|
ENST00000612663.4:c.*153A>G
|
ENSP00000477997.2:n.*153A>G
|
|
|
NM_000043.4:c.806A>G , LRG_134t1:c.806A>G
|
NP_000034.1:p.Asp269Gly
|
|
|
NM_152871.2:c.743A>G
|
NP_690610.1:p.Asp248Gly
|
|
|
NM_152872.2:c.*118A>G
|
NP_690611.1:n.*118A>G
|
|
|
NR_028033.2:n.980A>G
|
|
|
|
NR_028034.2:n.842A>G
|
|
|
|
NR_028035.2:n.905A>G
|
|
|
|
NR_028036.2:n.1043A>G
|
|
|
|
XM_006717819.2:c.887A>G
|
XP_006717882.1:p.Asp296Gly
|
|
|
XM_011539764.1:c.968A>G
|
XP_011538066.1:p.Asp323Gly
|
|
|
XM_011539765.1:c.905A>G
|
XP_011538067.1:p.Asp302Gly
|
|
|
XM_011539766.1:c.887A>G
|
XP_011538068.1:p.Asp296Gly
|
|
|
XM_011539767.1:c.851A>G
|
XP_011538069.1:p.Asp284Gly
|
|
|
XR_945732.1:n.874A>G
|
|
|
|
XR_945733.1:n.811A>G
|
|
|
|
NM_000043.5:c.806A>G
|
NP_000034.1:p.Asp269Gly
|
|
|
NM_001320619.1:c.*129A>G
|
NP_001307548.1:n.*129A>G
|
|
|
NM_152871.3:c.743A>G
|
NP_690610.1:p.Asp248Gly
|
|
|
NM_152872.3:c.*118A>G
|
NP_690611.1:n.*118A>G
|
|
|
NR_028033.3:n.952A>G
|
|
|
|
NR_028034.3:n.814A>G
|
|
|
|
NR_028035.3:n.877A>G
|
|
|
|
NR_028036.3:n.1015A>G
|
|
|
|
NR_135313.1:n.932A>G
|
|
|
|
NR_135314.1:n.1115A>G
|
|
|
|
NR_135315.1:n.868A>G
|
|
|
|
XM_006717819.3:c.887A>G
|
XP_006717882.1:p.Asp296Gly
|
|
|
XM_011539764.2:c.968A>G
|
XP_011538066.1:p.Asp323Gly
|
|
|
XM_011539765.2:c.905A>G
|
XP_011538067.1:p.Asp302Gly
|
|
|
XM_011539766.2:c.887A>G
|
XP_011538068.1:p.Asp296Gly
|
|
|
XM_011539767.3:c.851A>G
|
XP_011538069.1:p.Asp284Gly
|
|
|
XR_945732.3:n.874A>G
|
|
|
|
XR_945733.2:n.811A>G
|
|
|
|
NM_000043.6:c.806A>G
MANE Select
|
NP_000034.1:p.Asp269Gly
|
|
|
NM_001320619.2:c.*129A>G
|
NP_001307548.1:n.*129A>G
|
|
|
NM_152871.4:c.743A>G
|
NP_690610.1:p.Asp248Gly
|
|
|
NM_152872.4:c.*118A>G
|
NP_690611.1:n.*118A>G
|
|
|
NR_028033.4:n.713A>G
|
|
|
|
NR_028034.4:n.575A>G
|
|
|
|
NR_028035.4:n.638A>G
|
|
|
|
NR_028036.4:n.776A>G
|
|
|
|
NR_135313.2:n.693A>G
|
|
|
|
NR_135314.2:n.972A>G
|
|
|
|
NR_135315.2:n.725A>G
|
|
|
