|
ENST00000524561.2:n.3820A>G
|
|
|
|
ENST00000528374.2:c.810A>G
|
|
|
|
ENST00000529967.6:n.2558A>G
|
|
|
|
ENST00000532220.2:n.3452A>G
|
|
|
|
ENST00000642611.2:n.5552A>G
|
|
|
|
ENST00000644057.2:n.795A>G
|
|
|
|
ENST00000645004.2:n.1718A>G
|
|
|
|
ENST00000682051.1:n.4381A>G
|
|
|
|
ENST00000682110.1:n.4434A>G
|
|
|
|
ENST00000682140.1:c.*5A>G
|
ENSP00000507829.1:n.*5A>G
|
|
|
ENST00000682185.1:n.5524A>G
|
|
|
|
ENST00000682204.1:c.*2357A>G
|
ENSP00000507094.1:n.*2357A>G
|
|
|
ENST00000682215.1:n.4801A>G
|
|
|
|
ENST00000682288.1:c.*2650A>G
|
ENSP00000507506.1:n.*2650A>G
|
|
|
ENST00000682442.1:n.4654A>G
|
|
|
|
ENST00000682528.1:n.4511A>G
|
|
|
|
ENST00000682673.1:n.4378A>G
|
|
|
|
ENST00000682805.1:n.4839A>G
|
|
|
|
ENST00000682965.1:c.*641A>G
|
ENSP00000508229.1:n.*641A>G
|
|
|
ENST00000683093.1:n.5518A>G
|
|
|
|
ENST00000683136.1:c.4102A>G
|
ENSP00000507768.1:p.Ile1368Val
|
|
|
ENST00000683153.1:n.4476A>G
|
|
|
|
ENST00000683365.1:n.4536A>G
|
|
|
|
ENST00000683377.1:n.4434A>G
|
|
|
|
ENST00000683456.1:c.*1356A>G
|
ENSP00000508318.1:n.*1356A>G
|
|
|
ENST00000683522.1:n.4434A>G
|
|
|
|
ENST00000683562.1:c.*2388A>G
|
ENSP00000508265.1:n.*2388A>G
|
|
|
ENST00000683693.1:n.5999A>G
|
|
|
|
ENST00000683725.1:c.4219A>G
|
ENSP00000507496.1:p.Ile1407Val
|
|
|
ENST00000684010.1:n.4429A>G
|
|
|
|
ENST00000684157.1:n.5419A>G
|
|
|
|
ENST00000684253.1:n.4337A>G
|
|
|
|
ENST00000684288.1:c.*2391A>G
|
ENSP00000507143.1:n.*2391A>G
|
|
|
ENST00000684313.1:n.3866A>G
|
|
|
|
ENST00000684332.1:n.4507A>G
|
|
|
|
ENST00000684371.1:n.4540A>G
|
|
|
|
ENST00000684404.1:n.5462A>G
|
|
|
|
ENST00000684442.1:n.4658A>G
|
|
|
|
ENST00000684555.1:c.*2431A>G
|
ENSP00000507705.1:n.*2431A>G
|
|
|
ENST00000684571.1:c.4060A>G
|
ENSP00000506935.1:p.Ile1354Val
|
|
|
ENST00000684593.1:c.*3924A>G
|
ENSP00000507005.1:n.*3924A>G
|
|
|
ENST00000684711.1:c.*2615A>G
|
ENSP00000506841.1:n.*2615A>G
|
|
|
ENST00000302539.9:c.4222A>G
|
ENSP00000303960.4:p.Ile1408Val
|
|
|
ENST00000389817.8:c.4219A>G
MANE Select
|
ENSP00000374467.4:p.Ile1407Val
|
|
|
ENST00000642271.1:c.4216A>G
|
ENSP00000493749.1:p.Ile1406Val
|
|
|
ENST00000642579.1:c.2273A>G
|
|
|
|
ENST00000642611.1:n.5437A>G
|
|
|
|
ENST00000642902.1:c.4001A>G
|
|
|
|
ENST00000643260.1:c.4219A>G
|
ENSP00000494450.1:p.Ile1407Val
|
|
|
ENST00000643562.1:c.*2341A>G
|
ENSP00000496124.1:n.*2341A>G
|
|
|
ENST00000643925.1:c.2859A>G
|
|
|
|
ENST00000644057.1:n.296A>G
|
|
|
|
ENST00000644484.1:c.*3605A>G
|
ENSP00000493558.1:n.*3605A>G
|
|
|
ENST00000644675.1:c.*2391A>G
|
ENSP00000494567.1:n.*2391A>G
|
|
|
ENST00000644757.1:c.*3202+566A>G
|
ENSP00000495085.1:n.*3202+566A>G
|
|
|
ENST00000644772.1:c.4285A>G
|
ENSP00000494321.1:p.Ile1429Val
|
|
|
ENST00000645004.1:n.1912A>G
|
|
|
|
ENST00000645076.1:c.3418A>G
|
|
|
|
ENST00000645417.1:c.1407A>G
|
|
|
|
ENST00000645744.1:c.*3964-60A>G
|
ENSP00000494564.1:n.*3964-60A>G
|
|
|
ENST00000645760.1:c.4640A>G
|
|
|
|
ENST00000645884.1:c.*1502A>G
|
ENSP00000495516.1:n.*1502A>G
|
|
|
ENST00000646003.1:c.*2301-60A>G
|
ENSP00000495259.1:n.*2301-60A>G
|
|
|
ENST00000646207.1:c.*3056A>G
|
ENSP00000495025.1:n.*3056A>G
|
|
|
ENST00000646276.1:c.*3623A>G
|
ENSP00000496070.1:n.*3623A>G
|
|
|
ENST00000646592.1:c.3525A>G
|
|
|
|
ENST00000646902.1:c.4186A>G
|
ENSP00000494101.1:p.Ile1396Val
|
|
|
ENST00000646993.1:c.*2761A>G
|
ENSP00000493720.1:n.*2761A>G
|
|
|
ENST00000647013.1:c.4225A>G
|
ENSP00000496741.1:n.4225A>G
|
|
|
ENST00000647015.1:c.3970A>G
|
ENSP00000495389.1:p.Ile1324Val
|
|
|
ENST00000647086.1:c.*3805A>G
|
ENSP00000493677.1:n.*3805A>G
|
|
|
ENST00000647158.1:c.*2506A>G
|
ENSP00000495744.1:n.*2506A>G
|
|
|
ENST00000302539.8:c.4222A>G
|
ENSP00000303960.4:p.Ile1408Val
|
|
|
ENST00000389817.7:c.4219A>G
|
ENSP00000374467.3:p.Ile1407Val
|
|
|
ENST00000525022.1:n.218A>G
|
|
|
|
ENST00000526037.5:n.83A>G
|
|
|
|
ENST00000526168.5:c.67-60A>G
|
|
|
|
ENST00000531642.5:c.55A>G
|
|
|
|
NM_000352.4:c.4219A>G
|
NP_000343.2:p.Ile1407Val
|
|
|
NM_001287174.1:c.4222A>G
|
NP_001274103.1:p.Ile1408Val
|
|
|
XM_011520331.1:c.4219A>G
|
XP_011518633.1:p.Ile1407Val
|
|
|
XM_011520332.1:c.4222A>G
|
XP_011518634.1:p.Ile1408Val
|
|
|
XM_011520333.1:c.2719A>G
|
XP_011518635.1:p.Ile907Val
|
|
|
XR_930890.1:n.4285A>G
|
|
|
|
NM_001351295.1:c.4285A>G
|
NP_001338224.1:p.Ile1429Val
|
|
|
NM_001351296.1:c.4219A>G
|
NP_001338225.1:p.Ile1407Val
|
|
|
NM_001351297.1:c.4216A>G
|
NP_001338226.1:p.Ile1406Val
|
|
|
NR_147094.1:n.4514A>G
|
|
|
|
XM_017018197.2:c.4288A>G
|
XP_016873686.1:p.Ile1430Val
|
|
|
XM_017018199.1:c.4285A>G
|
XP_016873688.1:p.Ile1429Val
|
|
|
XM_017018201.2:c.4288A>G
|
XP_016873690.1:p.Ile1430Val
|
|
|
XM_017018202.1:c.2785A>G
|
XP_016873691.1:p.Ile929Val
|
|
|
XM_017018204.1:c.2176A>G
|
XP_016873693.1:p.Ile726Val
|
|
|
XM_024448668.1:c.2587A>G
|
XP_024304436.1:p.Ile863Val
|
|
|
XR_001747945.2:n.4360A>G
|
|
|
|
XR_001747946.2:n.4291A>G
|
|
|
|
XR_002957189.1:n.6074A>G
|
|
|
|
NM_000352.6:c.4219A>G
MANE Select
|
NP_000343.2:p.Ile1407Val
|
|
|
NM_001287174.2:c.4222A>G
|
NP_001274103.1:p.Ile1408Val
|
|
|
NM_001351295.2:c.4285A>G
|
NP_001338224.1:p.Ile1429Val
|
|
|
NM_001351296.2:c.4219A>G
|
NP_001338225.1:p.Ile1407Val
|
|
|
NM_001351297.2:c.4216A>G
|
NP_001338226.1:p.Ile1406Val
|
|
|
NR_147094.2:n.4514A>G
|
|
|
|
NM_001287174.3:c.4222A>G
|
NP_001274103.1:p.Ile1408Val
|
|
