|
ENST00000419884.6:c.544A>G
|
|
|
|
ENST00000681993.1:n.1466A>G
|
|
|
|
ENST00000682154.1:n.1348A>G
|
|
|
|
ENST00000682303.1:c.*3625A>G
|
ENSP00000508325.1:n.*3625A>G
|
|
|
ENST00000682308.1:c.3839A>G
|
ENSP00000507056.1:p.Lys1280Arg
|
|
|
ENST00000682434.1:n.3469A>G
|
|
|
|
ENST00000682480.1:c.3932A>G
|
ENSP00000508344.1:p.Lys1311Arg
|
|
|
ENST00000682546.1:c.3911A>G
|
ENSP00000508188.1:p.Lys1304Arg
|
|
|
ENST00000682585.1:c.*42A>G
|
ENSP00000506885.1:n.*42A>G
|
|
|
ENST00000682607.1:c.2657A>G
|
|
|
|
ENST00000682612.1:c.752+2018A>G
|
|
|
|
ENST00000682696.1:c.14A>G
|
ENSP00000508411.1:p.Lys5Arg
|
|
|
ENST00000682779.1:c.3905A>G
|
ENSP00000507947.1:p.Lys1302Arg
|
|
|
ENST00000682885.1:c.3869A>G
|
ENSP00000508036.1:p.Lys1290Arg
|
|
|
ENST00000682933.1:n.4114A>G
|
|
|
|
ENST00000683002.1:c.766A>G
|
|
|
|
ENST00000683072.1:n.4498A>G
|
|
|
|
ENST00000683080.1:n.1533A>G
|
|
|
|
ENST00000683096.1:n.2355A>G
|
|
|
|
ENST00000683125.1:c.4022A>G
|
ENSP00000507939.1:p.Lys1341Arg
|
|
|
ENST00000683213.1:c.3917A>G
|
ENSP00000507751.1:p.Lys1306Arg
|
|
|
ENST00000683220.1:c.3944A>G
|
ENSP00000507151.1:p.Lys1315Arg
|
|
|
ENST00000683329.1:n.4717A>G
|
|
|
|
ENST00000683346.1:c.*3789A>G
|
ENSP00000507458.1:n.*3789A>G
|
|
|
ENST00000683409.1:n.2446A>G
|
|
|
|
ENST00000683459.1:n.4501A>G
|
|
|
|
ENST00000683590.1:c.3587A>G
|
ENSP00000506820.1:p.Lys1196Arg
|
|
|
ENST00000683623.1:c.3821A>G
|
ENSP00000507702.1:p.Lys1274Arg
|
|
|
ENST00000683796.1:c.*3711A>G
|
ENSP00000508221.1:n.*3711A>G
|
|
|
ENST00000683833.1:c.3830A>G
|
ENSP00000506852.1:p.Lys1277Arg
|
|
|
ENST00000683994.1:c.*27A>G
|
ENSP00000507181.1:n.*27A>G
|
|
|
ENST00000684290.1:c.*1375A>G
|
ENSP00000507243.1:n.*1375A>G
|
|
|
ENST00000684306.1:c.*3827A>G
|
ENSP00000508384.1:n.*3827A>G
|
|
|
ENST00000684383.1:c.*3552A>G
|
ENSP00000506863.1:n.*3552A>G
|
|
|
ENST00000684418.1:n.5095A>G
|
|
|
|
ENST00000684433.1:n.298A>G
|
|
|
|
ENST00000684454.1:n.7778A>G
|
|
|
|
ENST00000684619.1:c.*3786A>G
|
ENSP00000508088.1:n.*3786A>G
|
|
|
ENST00000684743.1:n.6659A>G
|
|
|
|
ENST00000260665.12:c.3914A>G
MANE Select
|
ENSP00000260665.7:p.Lys1305Arg
|
|
|
ENST00000260665.11:c.3914A>G
|
ENSP00000260665.7:p.Lys1305Arg
|
|
|
ENST00000419884.5:c.155A>G
|
ENSP00000414207.1:p.Lys52Arg
|
|
|
ENST00000463456.5:n.2957A>G
|
|
|
|
NM_133259.3:c.3914A>G
|
NP_573566.2:p.Lys1305Arg
|
|
|
XM_006711915.2:c.3836A>G
|
XP_006711978.1:p.Lys1279Arg
|
|
|
XM_011532473.1:c.3839A>G
|
XP_011530775.1:p.Lys1280Arg
|
|
|
XM_011532474.1:c.3914A>G
|
XP_011530776.1:p.Lys1305Arg
|
|
|
XM_017003117.1:c.3761A>G
|
XP_016858606.1:p.Lys1254Arg
|
|
|
XR_002958896.1:n.3956A>G
|
|
|
|
NM_133259.4:c.3914A>G
MANE Select
|
NP_573566.2:p.Lys1305Arg
|
|
