ENST00000349036.9:c.2142-3577A>C
|
ENSP00000265621.6:n.2142-3577A>C
|
|
ENST00000419558.7:c.*116-3577A>C
|
ENSP00000416234.2:n.*116-3577A>C
|
|
ENST00000423897.7:c.2192A>C
|
ENSP00000412356.2:p.Ter731Ser
|
|
ENST00000453292.7:c.854-3574A>C
|
ENSP00000392000.2:n.854-3574A>C
|
|
ENST00000462499.6:c.36-3574A>C
|
ENSP00000499758.2:n.36-3574A>C
|
|
ENST00000464624.7:c.*99+969A>C
|
ENSP00000499607.2:n.*99+969A>C
|
|
ENST00000464788.6:c.80+969A>C
|
ENSP00000499239.2:n.80+969A>C
|
|
ENST00000467227.6:c.36-3574A>C
|
ENSP00000499681.2:n.36-3574A>C
|
|
ENST00000467321.6:c.80+969A>C
|
ENSP00000499523.2:n.80+969A>C
|
|
ENST00000468895.6:c.257+969A>C
|
ENSP00000499551.2:n.257+969A>C
|
|
ENST00000469431.6:c.80+969A>C
|
ENSP00000499654.2:n.80+969A>C
|
|
ENST00000470512.6:c.80+969A>C
|
ENSP00000499552.2:n.80+969A>C
|
|
ENST00000472183.6:c.80+969A>C
|
ENSP00000499673.2:n.80+969A>C
|
|
ENST00000476935.6:c.36-3577A>C
|
ENSP00000499409.2:n.36-3577A>C
|
|
ENST00000478585.6:c.36-3574A>C
|
ENSP00000499762.2:n.36-3574A>C
|
|
ENST00000480232.6:c.80+969A>C
|
ENSP00000499545.2:n.80+969A>C
|
|
ENST00000481039.6:c.36-3574A>C
|
ENSP00000499767.2:n.36-3574A>C
|
|
ENST00000482112.6:c.36-3577A>C
|
ENSP00000499794.2:n.36-3577A>C
|
|
ENST00000483387.2:n.761A>C
|
|
|
ENST00000485673.6:c.36-3574A>C
|
ENSP00000499334.2:n.36-3574A>C
|
|
ENST00000488546.6:c.36-3574A>C
|
ENSP00000499332.2:n.36-3574A>C
|
|
ENST00000488652.6:c.80+969A>C
|
ENSP00000499435.2:n.80+969A>C
|
|
ENST00000492907.6:c.36-3574A>C
|
ENSP00000499443.2:n.36-3574A>C
|
|
ENST00000603546.2:c.80+969A>C
|
ENSP00000474802.2:n.80+969A>C
|
|
ENST00000604005.6:c.80+969A>C
|
ENSP00000474219.2:n.80+969A>C
|
|
ENST00000663479.2:c.80+969A>C
|
ENSP00000499353.2:n.80+969A>C
|
|
ENST00000667293.2:c.80+969A>C
|
ENSP00000499293.2:n.80+969A>C
|
|
ENST00000676826.2:c.2186+969A>C
|
ENSP00000504675.2:n.2186+969A>C
|
|
ENST00000682134.1:n.2183+969A>C
|
|
|
ENST00000682803.1:c.-71+792A>C
|
ENSP00000507069.1:n.-71+792A>C
|
|
ENST00000682829.1:n.2586-3577A>C
|
|
|
ENST00000683015.1:c.1027+969A>C
|
ENSP00000506815.1:n.1027+969A>C
|
|
ENST00000684284.1:n.2635+969A>C
|
|
|
ENST00000306090.12:c.161+969A>C
|
ENSP00000304472.12:n.161+969A>C
|
|
ENST00000338783.7:c.218A>C
|
ENSP00000345971.7:p.Ter73Ser
|
|
ENST00000349036.8:c.2142-3577A>C
|
ENSP00000265621.5:n.2142-3577A>C
|
|
ENST00000354359.12:c.257+969A>C
|
ENSP00000346328.7:n.257+969A>C
|
|
ENST00000371085.8:c.257+969A>C
MANE Select
|
ENSP00000360126.3:n.257+969A>C
|
|
ENST00000371100.9:c.2186+969A>C
MANE Plus Clinical
|
ENSP00000360141.3:n.2186+969A>C
|
|
ENST00000419558.6:c.*116-3577A>C
|
ENSP00000416234.2:n.*116-3577A>C
|
|
ENST00000423897.6:c.2192A>C
|
ENSP00000412356.2:p.Ter731Ser
|
|
ENST00000453292.6:c.*116-3574A>C
|
ENSP00000392000.2:n.*116-3574A>C
|
|
ENST00000461152.6:c.983-3574A>C
|
ENSP00000499274.1:n.983-3574A>C
|
|
ENST00000481768.6:c.*91A>C
|
ENSP00000499644.2:n.*91A>C
|
|
ENST00000490374.6:n.346A>C
|
|
|
ENST00000657090.1:c.80+969A>C
|
ENSP00000499380.1:n.80+969A>C
|
|
ENST00000663479.1:c.80+969A>C
|
ENSP00000499353.1:n.80+969A>C
|
|
ENST00000667293.1:c.128+969A>C
|
ENSP00000499293.1:n.128+969A>C
|
|
ENST00000676826.1:c.2186+969A>C
|
ENSP00000504675.1:n.2186+969A>C
|
|
ENST00000265620.11:c.213-3577A>C
|
ENSP00000265620.7:n.213-3577A>C
|
|
ENST00000306090.11:c.93+8135A>C
|
ENSP00000304472.11:n.93+8135A>C
|
|
ENST00000313949.11:c.*160+969A>C
|
ENSP00000323571.7:n.*160+969A>C
|
|
ENST00000338783.6:c.185A>C
|
ENSP00000345971.6:p.Ter62Ser
|
|
ENST00000349036.7:c.305+969A>C
|
ENSP00000265621.4:n.305+969A>C
|
|
ENST00000354359.11:c.257+969A>C
|
ENSP00000346328.7:n.257+969A>C
|
|
ENST00000371075.7:c.*160+969A>C
MANE Plus Clinical
|
ENSP00000360115.3:n.*160+969A>C
|
|
ENST00000371081.5:c.263A>C
|
ENSP00000360122.1:p.Ter88Ser
|
|
ENST00000371085.7:c.257+969A>C
|
ENSP00000360126.3:n.257+969A>C
|
|
ENST00000371095.7:c.213-3574A>C
|
ENSP00000360136.3:n.213-3574A>C
|
|
ENST00000371098.6:c.*166A>C
|
ENSP00000360139.2:n.*166A>C
|
|
ENST00000371100.8:c.2186+969A>C
|
ENSP00000360141.3:n.2186+969A>C
|
|
ENST00000371102.8:c.2142-3574A>C
|
ENSP00000360143.4:n.2142-3574A>C
|
|
ENST00000419558.5:c.457-3577A>C
|
|
|
ENST00000423897.5:c.280A>C
|
|
|
ENST00000450130.5:c.301-3577A>C
|
|
|
ENST00000453292.5:c.617-3574A>C
|
ENSP00000392000.1:n.617-3574A>C
|
|
ENST00000461152.5:n.221-3574A>C
|
|
|
ENST00000462499.5:n.332-3574A>C
|
|
|
ENST00000464624.6:n.2473+969A>C
|
|
|
ENST00000464788.5:n.185+969A>C
|
|
|
ENST00000464960.5:n.530A>C
|
|
|
ENST00000467227.5:n.196-3574A>C
|
|
|
ENST00000467321.5:n.272+969A>C
|
|
|
ENST00000468895.5:n.124-3574A>C
|
|
|
ENST00000469431.5:n.374+969A>C
|
|
|
ENST00000470512.5:n.328+969A>C
|
|
|
ENST00000472183.5:n.509+969A>C
|
|
|
ENST00000476935.5:n.247-3577A>C
|
|
|
ENST00000477931.5:n.372+969A>C
|
|
|
ENST00000478585.5:n.268-3574A>C
|
|
|
ENST00000480232.5:n.273+969A>C
|
|
|
ENST00000480975.5:n.257-3577A>C
|
|
|
ENST00000481039.5:n.174+969A>C
|
|
|
ENST00000481768.5:n.1447A>C
|
|
|
ENST00000482112.5:n.332-3577A>C
|
|
|
ENST00000483387.1:n.567+969A>C
|
|
|
ENST00000484504.5:n.206A>C
|
|
|
ENST00000485673.5:n.500-3574A>C
|
|
|
ENST00000487862.5:n.489-3574A>C
|
|
|
ENST00000488546.5:n.114-3574A>C
|
|
|
ENST00000488652.5:n.347+969A>C
|
|
|
ENST00000490374.5:n.372+969A>C
|
|
|
ENST00000491348.5:n.612A>C
|
|
|
ENST00000492907.5:n.206-3574A>C
|
|
|
ENST00000493744.5:n.356A>C
|
|
|
ENST00000496934.5:n.1546+969A>C
|
|
|
ENST00000603546.1:c.80+969A>C
|
ENSP00000474802.1:n.80+969A>C
|
|
ENST00000604005.5:c.80+969A>C
|
ENSP00000474219.1:n.80+969A>C
|
|
NM_000516.4:c.257+969A>C
|
NP_000507.1:n.257+969A>C
|
|
NM_000516.5:c.257+969A>C
|
NP_000507.1:n.257+969A>C
|
|
NM_001077488.2:c.257+969A>C
|
NP_001070956.1:n.257+969A>C
|
|
NM_001077488.3:c.257+969A>C
|
NP_001070956.1:n.257+969A>C
|
|
NM_001077489.2:c.213-3577A>C
|
NP_001070957.1:n.213-3577A>C
|
|
NM_001077489.3:c.213-3577A>C
|
NP_001070957.1:n.213-3577A>C
|
|
NM_001077490.1:c.*118+969A>C
|
NP_001070958.1:n.*118+969A>C
|
|
NM_001077490.2:c.*118+969A>C
|
NP_001070958.1:n.*118+969A>C
|
|
NM_001309840.1:c.80+969A>C
|
NP_001296769.1:n.80+969A>C
|
|
NM_001309842.1:c.263A>C
|
NP_001296771.1:p.Ter88Ser
|
|
NM_001309861.1:c.80+969A>C
|
NP_001296790.1:n.80+969A>C
|
|
NM_001309883.1:c.*282A>C
|
NP_001296812.1:n.*282A>C
|
|
NM_016592.2:c.*160+969A>C
|
NP_057676.1:n.*160+969A>C
|
|
NM_016592.3:c.*160+969A>C
|
NP_057676.1:n.*160+969A>C
|
|
NM_080425.2:c.2186+969A>C
|
NP_536350.2:n.2186+969A>C
|
|
NM_080425.3:c.2186+969A>C
|
NP_536350.2:n.2186+969A>C
|
|
NM_080426.2:c.213-3574A>C
|
NP_536351.1:n.213-3574A>C
|
|
NM_080426.3:c.213-3574A>C
|
NP_536351.1:n.213-3574A>C
|
|
NR_003259.1:c.-4294966949+969A>C
|
|
|
NR_132272.1:n.170A>C
|
|
|
NR_132273.1:n.530A>C
|
|
|
XM_017027812.2:c.2186+969A>C
|
XP_016883301.1:n.2186+969A>C
|
|
XM_017027813.2:c.2142-3574A>C
|
XP_016883302.1:n.2142-3574A>C
|
|
XM_017027814.2:c.2142-3577A>C
|
XP_016883303.1:n.2142-3577A>C
|
|
XM_017027815.1:c.117-3577A>C
|
XP_016883304.1:n.117-3577A>C
|
|
XM_017027816.1:c.-42A>C
|
XP_016883305.1:n.-42A>C
|
|
XM_017027817.1:c.36-3577A>C
|
XP_016883306.1:n.36-3577A>C
|
|
XM_017027818.2:c.36-3577A>C
|
XP_016883307.1:n.36-3577A>C
|
|
XM_017027819.1:c.36-3577A>C
|
XP_016883308.1:n.36-3577A>C
|
|
XM_017027820.1:c.-42A>C
|
XP_016883309.1:n.-42A>C
|
|
XM_017027821.1:c.*160+969A>C
|
XP_016883310.1:n.*160+969A>C
|
|
XM_017027822.1:c.*116-3577A>C
|
XP_016883311.1:n.*116-3577A>C
|
|
XM_024451872.1:c.161+969A>C
|
XP_024307640.1:n.161+969A>C
|
|
XM_024451873.1:c.80+969A>C
|
XP_024307641.1:n.80+969A>C
|
|
XM_024451874.1:c.80+969A>C
|
XP_024307642.1:n.80+969A>C
|
|
XM_024451875.1:c.80+969A>C
|
XP_024307643.1:n.80+969A>C
|
|
XR_002958471.1:n.888A>C
|
|
|
NM_000516.6:c.257+969A>C
|
NP_000507.1:n.257+969A>C
|
|
NM_001077488.4:c.257+969A>C
|
NP_001070956.1:n.257+969A>C
|
|
NM_001077489.4:c.213-3577A>C
|
NP_001070957.1:n.213-3577A>C
|
|
NM_001309840.2:c.80+969A>C
|
NP_001296769.1:n.80+969A>C
|
|
NM_001309842.2:c.263A>C
|
NP_001296771.1:p.Ter88Ser
|
|
NM_001309861.2:c.80+969A>C
|
NP_001296790.1:n.80+969A>C
|
|
NM_016592.4:c.*160+969A>C
|
NP_057676.1:n.*160+969A>C
|
|
NM_080426.4:c.213-3574A>C
|
NP_536351.1:n.213-3574A>C
|
|
NR_132272.2:n.171A>C
|
|
|
NM_000516.7:c.257+969A>C
MANE Select
|
NP_000507.1:n.257+969A>C
|
|
NM_001077488.5:c.257+969A>C
|
NP_001070956.1:n.257+969A>C
|
|
NM_001077490.3:c.*118+969A>C
|
NP_001070958.1:n.*118+969A>C
|
|
NM_016592.5:c.*160+969A>C
MANE Plus Clinical
|
NP_057676.1:n.*160+969A>C
|
|
NM_080425.4:c.2186+969A>C
MANE Plus Clinical
|
NP_536350.2:n.2186+969A>C
|
|