|
ENST00000524561.2:n.4298T>G
|
|
|
|
ENST00000526037.6:n.632T>G
|
|
|
|
ENST00000528374.2:c.1288T>G
|
|
|
|
ENST00000529967.6:n.3036T>G
|
|
|
|
ENST00000532220.2:n.3930T>G
|
|
|
|
ENST00000642611.2:n.6030T>G
|
|
|
|
ENST00000644057.2:n.1273T>G
|
|
|
|
ENST00000645004.2:n.2196T>G
|
|
|
|
ENST00000682051.1:n.4859T>G
|
|
|
|
ENST00000682110.1:n.4912T>G
|
|
|
|
ENST00000682140.1:c.*483T>G
|
ENSP00000507829.1:n.*483T>G
|
|
|
ENST00000682185.1:n.6002T>G
|
|
|
|
ENST00000682204.1:c.*2835T>G
|
ENSP00000507094.1:n.*2835T>G
|
|
|
ENST00000682215.1:n.5279T>G
|
|
|
|
ENST00000682288.1:c.*3128T>G
|
ENSP00000507506.1:n.*3128T>G
|
|
|
ENST00000682442.1:n.5132T>G
|
|
|
|
ENST00000682528.1:n.4989T>G
|
|
|
|
ENST00000682673.1:n.4856T>G
|
|
|
|
ENST00000682805.1:n.5317T>G
|
|
|
|
ENST00000682965.1:c.*1119T>G
|
ENSP00000508229.1:n.*1119T>G
|
|
|
ENST00000683093.1:n.5892T>G
|
|
|
|
ENST00000683136.1:c.4580T>G
|
ENSP00000507768.1:p.Leu1527Arg
|
|
|
ENST00000683153.1:n.4954T>G
|
|
|
|
ENST00000683365.1:n.5014T>G
|
|
|
|
ENST00000683377.1:n.4808T>G
|
|
|
|
ENST00000683456.1:c.*1834T>G
|
ENSP00000508318.1:n.*1834T>G
|
|
|
ENST00000683522.1:n.4994T>G
|
|
|
|
ENST00000683562.1:c.*2762T>G
|
ENSP00000508265.1:n.*2762T>G
|
|
|
ENST00000683693.1:n.6373T>G
|
|
|
|
ENST00000683725.1:c.*162T>G
|
ENSP00000507496.1:n.*162T>G
|
|
|
ENST00000684010.1:n.4907T>G
|
|
|
|
ENST00000684014.1:n.884T>G
|
|
|
|
ENST00000684157.1:n.5897T>G
|
|
|
|
ENST00000684253.1:n.4815T>G
|
|
|
|
ENST00000684288.1:c.*2869T>G
|
ENSP00000507143.1:n.*2869T>G
|
|
|
ENST00000684313.1:n.4344T>G
|
|
|
|
ENST00000684332.1:n.4985T>G
|
|
|
|
ENST00000684371.1:n.5018T>G
|
|
|
|
ENST00000684404.1:n.5940T>G
|
|
|
|
ENST00000684442.1:n.5136T>G
|
|
|
|
ENST00000684555.1:c.*2909T>G
|
ENSP00000507705.1:n.*2909T>G
|
|
|
ENST00000684571.1:c.4538T>G
|
ENSP00000506935.1:p.Leu1513Arg
|
|
|
ENST00000684593.1:c.*4402T>G
|
ENSP00000507005.1:n.*4402T>G
|
|
|
ENST00000684711.1:c.*3093T>G
|
ENSP00000506841.1:n.*3093T>G
|
|
|
ENST00000302539.9:c.4700T>G
|
ENSP00000303960.4:p.Leu1567Arg
|
|
|
ENST00000389817.8:c.4697T>G
MANE Select
|
ENSP00000374467.4:p.Leu1566Arg
|
|
|
ENST00000642271.1:c.4694T>G
|
ENSP00000493749.1:p.Leu1565Arg
|
|
|
ENST00000642579.1:c.2751T>G
|
|
|
|
ENST00000642611.1:n.5915T>G
|
|
|
|
ENST00000642902.1:c.4479T>G
|
|
|
|
ENST00000643260.1:c.4697T>G
|
ENSP00000494450.1:p.Leu1566Arg
|
|
|
ENST00000643562.1:c.*2819T>G
|
ENSP00000496124.1:n.*2819T>G
|
|
|
ENST00000643925.1:c.3274T>G
|
|
|
|
ENST00000644057.1:n.856T>G
|
|
|
|
ENST00000644484.1:c.*4083T>G
|
ENSP00000493558.1:n.*4083T>G
|
|
|
ENST00000644675.1:c.*2869T>G
|
ENSP00000494567.1:n.*2869T>G
|
|
|
ENST00000644757.1:c.*3203-60T>G
|
ENSP00000495085.1:n.*3203-60T>G
|
|
|
ENST00000644772.1:c.4763T>G
|
ENSP00000494321.1:p.Leu1588Arg
|
|
|
ENST00000645004.1:n.2390T>G
|
|
|
|
ENST00000645076.1:c.3792T>G
|
|
|
|
ENST00000645760.1:c.5118T>G
|
|
|
|
ENST00000645884.1:c.*1980T>G
|
ENSP00000495516.1:n.*1980T>G
|
|
|
ENST00000646003.1:c.*2719T>G
|
ENSP00000495259.1:n.*2719T>G
|
|
|
ENST00000646207.1:c.*3534T>G
|
ENSP00000495025.1:n.*3534T>G
|
|
|
ENST00000646592.1:c.4003T>G
|
|
|
|
ENST00000646902.1:c.4664T>G
|
ENSP00000494101.1:p.Leu1555Arg
|
|
|
ENST00000646993.1:c.*3135T>G
|
ENSP00000493720.1:n.*3135T>G
|
|
|
ENST00000647015.1:c.4448T>G
|
ENSP00000495389.1:p.Leu1483Arg
|
|
|
ENST00000647086.1:c.*4283T>G
|
ENSP00000493677.1:n.*4283T>G
|
|
|
ENST00000302539.8:c.4700T>G
|
ENSP00000303960.4:p.Leu1567Arg
|
|
|
ENST00000389817.7:c.4697T>G
|
ENSP00000374467.3:p.Leu1566Arg
|
|
|
ENST00000526037.5:n.457T>G
|
|
|
|
ENST00000526168.5:c.485T>G
|
|
|
|
ENST00000531642.5:c.728T>G
|
|
|
|
NM_000352.4:c.4697T>G
|
NP_000343.2:p.Leu1566Arg
|
|
|
NM_001287174.1:c.4700T>G
|
NP_001274103.1:p.Leu1567Arg
|
|
|
XM_011520331.1:c.4697T>G
|
XP_011518633.1:p.Leu1566Arg
|
|
|
XM_011520333.1:c.3197T>G
|
XP_011518635.1:p.Leu1066Arg
|
|
|
XR_930890.1:n.4659T>G
|
|
|
|
NM_001351295.1:c.4763T>G
|
NP_001338224.1:p.Leu1588Arg
|
|
|
NM_001351296.1:c.4697T>G
|
NP_001338225.1:p.Leu1566Arg
|
|
|
NM_001351297.1:c.4694T>G
|
NP_001338226.1:p.Leu1565Arg
|
|
|
NR_147094.1:n.4992T>G
|
|
|
|
XM_017018197.2:c.4766T>G
|
XP_016873686.1:p.Leu1589Arg
|
|
|
XM_017018199.1:c.4763T>G
|
XP_016873688.1:p.Leu1588Arg
|
|
|
XM_017018202.1:c.3263T>G
|
XP_016873691.1:p.Leu1088Arg
|
|
|
XM_017018204.1:c.2654T>G
|
XP_016873693.1:p.Leu885Arg
|
|
|
XM_024448668.1:c.3065T>G
|
XP_024304436.1:p.Leu1022Arg
|
|
|
XR_001747945.2:n.4734T>G
|
|
|
|
XR_001747946.2:n.4665T>G
|
|
|
|
XR_002957189.1:n.6448T>G
|
|
|
|
NM_000352.6:c.4697T>G
MANE Select
|
NP_000343.2:p.Leu1566Arg
|
|
|
NM_001287174.2:c.4700T>G
|
NP_001274103.1:p.Leu1567Arg
|
|
|
NM_001351295.2:c.4763T>G
|
NP_001338224.1:p.Leu1588Arg
|
|
|
NM_001351296.2:c.4697T>G
|
NP_001338225.1:p.Leu1566Arg
|
|
|
NM_001351297.2:c.4694T>G
|
NP_001338226.1:p.Leu1565Arg
|
|
|
NR_147094.2:n.4992T>G
|
|
|
|
NM_001287174.3:c.4700T>G
|
NP_001274103.1:p.Leu1567Arg
|
|
