|
ENST00000524561.2:n.3598C>G
|
|
|
|
ENST00000528374.2:c.588C>G
|
|
|
|
ENST00000529967.6:n.2336C>G
|
|
|
|
ENST00000532220.2:n.2245C>G
|
|
|
|
ENST00000642611.2:n.4212C>G
|
|
|
|
ENST00000644057.2:n.440C>G
|
|
|
|
ENST00000645004.2:n.1496C>G
|
|
|
|
ENST00000682051.1:n.4159C>G
|
|
|
|
ENST00000682110.1:n.4212C>G
|
|
|
|
ENST00000682140.1:c.3985+155C>G
|
ENSP00000507829.1:n.3985+155C>G
|
|
|
ENST00000682185.1:n.5302C>G
|
|
|
|
ENST00000682204.1:c.*2135C>G
|
ENSP00000507094.1:n.*2135C>G
|
|
|
ENST00000682215.1:n.4579C>G
|
|
|
|
ENST00000682288.1:c.*2428C>G
|
ENSP00000507506.1:n.*2428C>G
|
|
|
ENST00000682442.1:n.4432C>G
|
|
|
|
ENST00000682528.1:n.4289C>G
|
|
|
|
ENST00000682673.1:n.4156C>G
|
|
|
|
ENST00000682805.1:n.4579C>G
|
|
|
|
ENST00000682965.1:c.*419C>G
|
ENSP00000508229.1:n.*419C>G
|
|
|
ENST00000683093.1:n.4311C>G
|
|
|
|
ENST00000683136.1:c.3880C>G
|
ENSP00000507768.1:p.Leu1294Val
|
|
|
ENST00000683153.1:n.4254C>G
|
|
|
|
ENST00000683365.1:n.4314C>G
|
|
|
|
ENST00000683377.1:n.4212C>G
|
|
|
|
ENST00000683456.1:c.*1134C>G
|
ENSP00000508318.1:n.*1134C>G
|
|
|
ENST00000683522.1:n.4212C>G
|
|
|
|
ENST00000683562.1:c.*2166C>G
|
ENSP00000508265.1:n.*2166C>G
|
|
|
ENST00000683693.1:n.4659C>G
|
|
|
|
ENST00000683725.1:c.3997C>G
|
ENSP00000507496.1:p.Leu1333Val
|
|
|
ENST00000684010.1:n.4207C>G
|
|
|
|
ENST00000684157.1:n.4212C>G
|
|
|
|
ENST00000684253.1:n.4115C>G
|
|
|
|
ENST00000684288.1:c.*2169C>G
|
ENSP00000507143.1:n.*2169C>G
|
|
|
ENST00000684313.1:n.3644C>G
|
|
|
|
ENST00000684332.1:n.4285C>G
|
|
|
|
ENST00000684371.1:n.4318C>G
|
|
|
|
ENST00000684404.1:n.4255C>G
|
|
|
|
ENST00000684442.1:n.4436C>G
|
|
|
|
ENST00000684555.1:c.*2209C>G
|
ENSP00000507705.1:n.*2209C>G
|
|
|
ENST00000684571.1:c.3838C>G
|
ENSP00000506935.1:p.Leu1280Val
|
|
|
ENST00000684593.1:c.*3702C>G
|
ENSP00000507005.1:n.*3702C>G
|
|
|
ENST00000684711.1:c.*2393C>G
|
ENSP00000506841.1:n.*2393C>G
|
|
|
ENST00000302539.9:c.4000C>G
|
ENSP00000303960.4:p.Leu1334Val
|
|
|
ENST00000389817.8:c.3997C>G
MANE Select
|
ENSP00000374467.4:p.Leu1333Val
|
|
|
ENST00000642271.1:c.3994C>G
|
ENSP00000493749.1:p.Leu1332Val
|
|
|
ENST00000642579.1:c.2073-22C>G
|
|
|
|
ENST00000642611.1:n.4097C>G
|
|
|
|
ENST00000642902.1:c.3779C>G
|
|
|
|
ENST00000643260.1:c.3997C>G
|
ENSP00000494450.1:p.Leu1333Val
|
|
|
ENST00000643562.1:c.*2119C>G
|
ENSP00000496124.1:n.*2119C>G
|
|
|
ENST00000643925.1:c.2637C>G
|
|
|
|
ENST00000644057.1:n.74C>G
|
|
|
|
ENST00000644484.1:c.*2398C>G
|
ENSP00000493558.1:n.*2398C>G
|
|
|
ENST00000644675.1:c.*2169C>G
|
ENSP00000494567.1:n.*2169C>G
|
|
|
ENST00000644757.1:c.*2428C>G
|
ENSP00000495085.1:n.*2428C>G
|
|
|
ENST00000644772.1:c.4063C>G
|
ENSP00000494321.1:p.Leu1355Val
|
|
|
ENST00000645004.1:n.1652C>G
|
|
|
|
ENST00000645076.1:c.3196C>G
|
|
|
|
ENST00000645417.1:c.1185C>G
|
|
|
|
ENST00000645744.1:c.*2777C>G
|
ENSP00000494564.1:n.*2777C>G
|
|
|
ENST00000645760.1:c.4418C>G
|
|
|
|
ENST00000645884.1:c.*1280C>G
|
ENSP00000495516.1:n.*1280C>G
|
|
|
ENST00000646003.1:c.*2099C>G
|
ENSP00000495259.1:n.*2099C>G
|
|
|
ENST00000646207.1:c.*2834C>G
|
ENSP00000495025.1:n.*2834C>G
|
|
|
ENST00000646276.1:c.*2416C>G
|
ENSP00000496070.1:n.*2416C>G
|
|
|
ENST00000646592.1:c.3303C>G
|
|
|
|
ENST00000646902.1:c.3986-22C>G
|
ENSP00000494101.1:n.3986-22C>G
|
|
|
ENST00000646993.1:c.*2539C>G
|
ENSP00000493720.1:n.*2539C>G
|
|
|
ENST00000647013.1:c.4003C>G
|
ENSP00000496741.1:n.4003C>G
|
|
|
ENST00000647015.1:c.3748C>G
|
ENSP00000495389.1:p.Leu1250Val
|
|
|
ENST00000647086.1:c.*3605-22C>G
|
ENSP00000493677.1:n.*3605-22C>G
|
|
|
ENST00000647158.1:c.*2284C>G
|
ENSP00000495744.1:n.*2284C>G
|
|
|
ENST00000302539.8:c.4000C>G
|
ENSP00000303960.4:p.Leu1334Val
|
|
|
ENST00000389817.7:c.3997C>G
|
ENSP00000374467.3:p.Leu1333Val
|
|
|
ENST00000527905.5:c.*1019C>G
|
ENSP00000431653.1:n.*1019C>G
|
|
|
ENST00000528374.1:c.479C>G
|
|
|
|
ENST00000531137.1:n.562C>G
|
|
|
|
ENST00000531891.1:c.357-22C>G
|
|
|
|
ENST00000532220.1:n.471C>G
|
|
|
|
NM_000352.4:c.3997C>G
|
NP_000343.2:p.Leu1333Val
|
|
|
NM_001287174.1:c.4000C>G
|
NP_001274103.1:p.Leu1334Val
|
|
|
XM_011520331.1:c.3997C>G
|
XP_011518633.1:p.Leu1333Val
|
|
|
XM_011520332.1:c.4000C>G
|
XP_011518634.1:p.Leu1334Val
|
|
|
XM_011520333.1:c.2497C>G
|
XP_011518635.1:p.Leu833Val
|
|
|
XR_930890.1:n.4063C>G
|
|
|
|
NM_001351295.1:c.4063C>G
|
NP_001338224.1:p.Leu1355Val
|
|
|
NM_001351296.1:c.3997C>G
|
NP_001338225.1:p.Leu1333Val
|
|
|
NM_001351297.1:c.3994C>G
|
NP_001338226.1:p.Leu1332Val
|
|
|
NR_147094.1:n.4292C>G
|
|
|
|
XM_017018197.2:c.4066C>G
|
XP_016873686.1:p.Leu1356Val
|
|
|
XM_017018199.1:c.4063C>G
|
XP_016873688.1:p.Leu1355Val
|
|
|
XM_017018201.2:c.4066C>G
|
XP_016873690.1:p.Leu1356Val
|
|
|
XM_017018202.1:c.2563C>G
|
XP_016873691.1:p.Leu855Val
|
|
|
XM_017018204.1:c.1954C>G
|
XP_016873693.1:p.Leu652Val
|
|
|
XM_024448668.1:c.2365C>G
|
XP_024304436.1:p.Leu789Val
|
|
|
XR_001747945.2:n.4138C>G
|
|
|
|
XR_001747946.2:n.4069C>G
|
|
|
|
XR_002957189.1:n.4734C>G
|
|
|
|
NM_000352.6:c.3997C>G
MANE Select
|
NP_000343.2:p.Leu1333Val
|
|
|
NM_001287174.2:c.4000C>G
|
NP_001274103.1:p.Leu1334Val
|
|
|
NM_001351295.2:c.4063C>G
|
NP_001338224.1:p.Leu1355Val
|
|
|
NM_001351296.2:c.3997C>G
|
NP_001338225.1:p.Leu1333Val
|
|
|
NM_001351297.2:c.3994C>G
|
NP_001338226.1:p.Leu1332Val
|
|
|
NR_147094.2:n.4292C>G
|
|
|
|
NM_001287174.3:c.4000C>G
|
NP_001274103.1:p.Leu1334Val
|
|
