|
ENST00000524561.2:n.1582A>G
|
|
|
|
ENST00000529967.6:n.13A>G
|
|
|
|
ENST00000642611.2:n.1979A>G
|
|
|
|
ENST00000682051.1:n.1926A>G
|
|
|
|
ENST00000682110.1:n.1979A>G
|
|
|
|
ENST00000682140.1:c.1910A>G
|
ENSP00000507829.1:p.Tyr637Cys
|
|
|
ENST00000682185.1:n.3218A>G
|
|
|
|
ENST00000682204.1:c.*51A>G
|
ENSP00000507094.1:n.*51A>G
|
|
|
ENST00000682215.1:n.1979A>G
|
|
|
|
ENST00000682288.1:c.*341A>G
|
ENSP00000507506.1:n.*341A>G
|
|
|
ENST00000682442.1:n.2100A>G
|
|
|
|
ENST00000682528.1:n.1979A>G
|
|
|
|
ENST00000682673.1:n.1926A>G
|
|
|
|
ENST00000682805.1:n.1979A>G
|
|
|
|
ENST00000682965.1:c.1910A>G
|
ENSP00000508229.1:p.Tyr637Cys
|
|
|
ENST00000683093.1:n.2081A>G
|
|
|
|
ENST00000683136.1:c.1910A>G
|
ENSP00000507768.1:p.Tyr637Cys
|
|
|
ENST00000683153.1:n.1979A>G
|
|
|
|
ENST00000683253.1:n.2995A>G
|
|
|
|
ENST00000683365.1:n.2081A>G
|
|
|
|
ENST00000683377.1:n.1979A>G
|
|
|
|
ENST00000683456.1:c.1910A>G
|
ENSP00000508318.1:p.Tyr637Cys
|
|
|
ENST00000683522.1:n.1979A>G
|
|
|
|
ENST00000683562.1:c.*82A>G
|
ENSP00000508265.1:n.*82A>G
|
|
|
ENST00000683693.1:n.1979A>G
|
|
|
|
ENST00000683725.1:c.1913A>G
|
ENSP00000507496.1:p.Tyr638Cys
|
|
|
ENST00000684010.1:n.1979A>G
|
|
|
|
ENST00000684157.1:n.1979A>G
|
|
|
|
ENST00000684253.1:n.1885A>G
|
|
|
|
ENST00000684288.1:c.*82A>G
|
ENSP00000507143.1:n.*82A>G
|
|
|
ENST00000684313.1:n.1724-11613A>G
|
|
|
|
ENST00000684332.1:n.2052A>G
|
|
|
|
ENST00000684371.1:n.1926A>G
|
|
|
|
ENST00000684404.1:n.1979A>G
|
|
|
|
ENST00000684442.1:n.1979A>G
|
|
|
|
ENST00000684555.1:c.*122A>G
|
ENSP00000507705.1:n.*122A>G
|
|
|
ENST00000684571.1:c.1754A>G
|
ENSP00000506935.1:p.Tyr585Cys
|
|
|
ENST00000684593.1:c.*1618A>G
|
ENSP00000507005.1:n.*1618A>G
|
|
|
ENST00000684711.1:c.*309A>G
|
ENSP00000506841.1:n.*309A>G
|
|
|
ENST00000302539.9:c.1913A>G
|
ENSP00000303960.4:p.Tyr638Cys
|
|
|
ENST00000389817.8:c.1913A>G
MANE Select
|
ENSP00000374467.4:p.Tyr638Cys
|
|
|
ENST00000532728.6:c.1494A>G
|
|
|
|
ENST00000642271.1:c.1910A>G
|
ENSP00000493749.1:p.Tyr637Cys
|
|
|
ENST00000642611.1:n.1864A>G
|
|
|
|
ENST00000642902.1:c.1748A>G
|
|
|
|
ENST00000643260.1:c.1910A>G
|
ENSP00000494450.1:p.Tyr637Cys
|
|
|
ENST00000643562.1:c.1913A>G
|
ENSP00000496124.1:p.Tyr638Cys
|
|
|
ENST00000644447.1:c.266A>G
|
ENSP00000496282.1:p.Tyr89Cys
|
|
|
ENST00000644472.1:c.*274A>G
|
ENSP00000495378.1:n.*274A>G
|
|
|
ENST00000644484.1:c.*122A>G
|
ENSP00000493558.1:n.*122A>G
|
|
|
ENST00000644542.1:c.*1615A>G
|
ENSP00000495532.1:n.*1615A>G
|
|
|
ENST00000644649.1:c.1083A>G
|
|
|
|
ENST00000644675.1:c.*82A>G
|
ENSP00000494567.1:n.*82A>G
|
|
|
ENST00000644757.1:c.*215A>G
|
ENSP00000495085.1:n.*215A>G
|
|
|
ENST00000644772.1:c.1913A>G
|
ENSP00000494321.1:p.Tyr638Cys
|
|
|
ENST00000645076.1:c.1165A>G
|
|
|
|
ENST00000645744.1:c.*274A>G
|
ENSP00000494564.1:n.*274A>G
|
|
|
ENST00000645760.1:c.2188A>G
|
|
|
|
ENST00000645884.1:c.1910A>G
|
ENSP00000495516.1:p.Tyr637Cys
|
|
|
ENST00000646003.1:c.*51A>G
|
ENSP00000495259.1:n.*51A>G
|
|
|
ENST00000646207.1:c.*274A>G
|
ENSP00000495025.1:n.*274A>G
|
|
|
ENST00000646276.1:c.*183A>G
|
ENSP00000496070.1:n.*183A>G
|
|
|
ENST00000646592.1:c.977A>G
|
|
|
|
ENST00000646902.1:c.1910A>G
|
ENSP00000494101.1:p.Tyr637Cys
|
|
|
ENST00000646993.1:c.*309A>G
|
ENSP00000493720.1:n.*309A>G
|
|
|
ENST00000647013.1:c.1916A>G
|
ENSP00000496741.1:n.1916A>G
|
|
|
ENST00000647015.1:c.1672-170A>G
|
ENSP00000495389.1:n.1672-170A>G
|
|
|
ENST00000647086.1:c.*1640A>G
|
ENSP00000493677.1:n.*1640A>G
|
|
|
ENST00000647158.1:c.*51A>G
|
ENSP00000495744.1:n.*51A>G
|
|
|
ENST00000302539.8:c.1913A>G
|
ENSP00000303960.4:p.Tyr638Cys
|
|
|
ENST00000389817.7:c.1913A>G
|
ENSP00000374467.3:p.Tyr638Cys
|
|
|
ENST00000527905.5:c.1883A>G
|
ENSP00000431653.1:p.Tyr628Cys
|
|
|
NM_000352.4:c.1913A>G
|
NP_000343.2:p.Tyr638Cys
|
|
|
NM_001287174.1:c.1913A>G
|
NP_001274103.1:p.Tyr638Cys
|
|
|
XM_011520331.1:c.1910A>G
|
XP_011518633.1:p.Tyr637Cys
|
|
|
XM_011520332.1:c.1913A>G
|
XP_011518634.1:p.Tyr638Cys
|
|
|
XM_011520333.1:c.410A>G
|
XP_011518635.1:p.Tyr137Cys
|
|
|
XM_011520334.1:c.1913A>G
|
XP_011518636.1:p.Tyr638Cys
|
|
|
XR_930890.1:n.1976A>G
|
|
|
|
XR_930891.1:n.1976A>G
|
|
|
|
XR_930892.1:n.1976A>G
|
|
|
|
XR_930893.1:n.1976A>G
|
|
|
|
NM_001351295.1:c.1913A>G
|
NP_001338224.1:p.Tyr638Cys
|
|
|
NM_001351296.1:c.1910A>G
|
NP_001338225.1:p.Tyr637Cys
|
|
|
NM_001351297.1:c.1910A>G
|
NP_001338226.1:p.Tyr637Cys
|
|
|
NR_147094.1:n.1979A>G
|
|
|
|
XM_017018197.2:c.1913A>G
|
XP_016873686.1:p.Tyr638Cys
|
|
|
XM_017018199.1:c.1910A>G
|
XP_016873688.1:p.Tyr637Cys
|
|
|
XM_017018201.2:c.1913A>G
|
XP_016873690.1:p.Tyr638Cys
|
|
|
XM_017018202.1:c.410A>G
|
XP_016873691.1:p.Tyr137Cys
|
|
|
XM_017018204.1:c.-131A>G
|
XP_016873693.1:n.-131A>G
|
|
|
XM_024448668.1:c.278A>G
|
XP_024304436.1:p.Tyr93Cys
|
|
|
XR_001747945.2:n.1985A>G
|
|
|
|
XR_001747946.2:n.1985A>G
|
|
|
|
XR_002957189.1:n.1985A>G
|
|
|
|
NM_000352.6:c.1913A>G
MANE Select
|
NP_000343.2:p.Tyr638Cys
|
|
|
NM_001287174.2:c.1913A>G
|
NP_001274103.1:p.Tyr638Cys
|
|
|
NM_001351295.2:c.1913A>G
|
NP_001338224.1:p.Tyr638Cys
|
|
|
NM_001351296.2:c.1910A>G
|
NP_001338225.1:p.Tyr637Cys
|
|
|
NM_001351297.2:c.1910A>G
|
NP_001338226.1:p.Tyr637Cys
|
|
|
NR_147094.2:n.1979A>G
|
|
|
|
NM_001287174.3:c.1913A>G
|
NP_001274103.1:p.Tyr638Cys
|
|
