|
ENST00000419884.6:c.596T>G
|
|
|
|
ENST00000681993.1:n.1518T>G
|
|
|
|
ENST00000682154.1:n.1400T>G
|
|
|
|
ENST00000682303.1:c.*3677T>G
|
ENSP00000508325.1:n.*3677T>G
|
|
|
ENST00000682308.1:c.3891T>G
|
ENSP00000507056.1:p.Asn1297Lys
|
|
|
ENST00000682434.1:n.3521T>G
|
|
|
|
ENST00000682480.1:c.3984T>G
|
ENSP00000508344.1:p.Asn1328Lys
|
|
|
ENST00000682546.1:c.3963T>G
|
ENSP00000508188.1:p.Asn1321Lys
|
|
|
ENST00000682585.1:c.*94T>G
|
ENSP00000506885.1:n.*94T>G
|
|
|
ENST00000682607.1:c.2709T>G
|
|
|
|
ENST00000682612.1:c.752+2070T>G
|
|
|
|
ENST00000682696.1:c.66T>G
|
ENSP00000508411.1:p.Asn22Lys
|
|
|
ENST00000682779.1:c.3957T>G
|
ENSP00000507947.1:p.Asn1319Lys
|
|
|
ENST00000682885.1:c.3921T>G
|
ENSP00000508036.1:p.Asn1307Lys
|
|
|
ENST00000682933.1:n.4166T>G
|
|
|
|
ENST00000683002.1:c.818T>G
|
|
|
|
ENST00000683072.1:n.4550T>G
|
|
|
|
ENST00000683080.1:n.1585T>G
|
|
|
|
ENST00000683096.1:n.2407T>G
|
|
|
|
ENST00000683125.1:c.4074T>G
|
ENSP00000507939.1:p.Asn1358Lys
|
|
|
ENST00000683213.1:c.3969T>G
|
ENSP00000507751.1:p.Asn1323Lys
|
|
|
ENST00000683220.1:c.3996T>G
|
ENSP00000507151.1:p.Asn1332Lys
|
|
|
ENST00000683329.1:n.4769T>G
|
|
|
|
ENST00000683346.1:c.*3841T>G
|
ENSP00000507458.1:n.*3841T>G
|
|
|
ENST00000683409.1:n.2498T>G
|
|
|
|
ENST00000683459.1:n.4553T>G
|
|
|
|
ENST00000683590.1:c.3639T>G
|
ENSP00000506820.1:p.Asn1213Lys
|
|
|
ENST00000683623.1:c.3873T>G
|
ENSP00000507702.1:p.Asn1291Lys
|
|
|
ENST00000683796.1:c.*3763T>G
|
ENSP00000508221.1:n.*3763T>G
|
|
|
ENST00000683833.1:c.3882T>G
|
ENSP00000506852.1:p.Asn1294Lys
|
|
|
ENST00000683994.1:c.*79T>G
|
ENSP00000507181.1:n.*79T>G
|
|
|
ENST00000684290.1:c.*1427T>G
|
ENSP00000507243.1:n.*1427T>G
|
|
|
ENST00000684306.1:c.*3879T>G
|
ENSP00000508384.1:n.*3879T>G
|
|
|
ENST00000684383.1:c.*3604T>G
|
ENSP00000506863.1:n.*3604T>G
|
|
|
ENST00000684418.1:n.5147T>G
|
|
|
|
ENST00000684433.1:n.350T>G
|
|
|
|
ENST00000684454.1:n.7830T>G
|
|
|
|
ENST00000684619.1:c.*3838T>G
|
ENSP00000508088.1:n.*3838T>G
|
|
|
ENST00000684743.1:n.6711T>G
|
|
|
|
ENST00000260665.12:c.3966T>G
MANE Select
|
ENSP00000260665.7:p.Asn1322Lys
|
|
|
ENST00000260665.11:c.3966T>G
|
ENSP00000260665.7:p.Asn1322Lys
|
|
|
ENST00000419884.5:c.207T>G
|
ENSP00000414207.1:p.Asn69Lys
|
|
|
ENST00000463456.5:n.3009T>G
|
|
|
|
NM_133259.3:c.3966T>G
|
NP_573566.2:p.Asn1322Lys
|
|
|
XM_006711915.2:c.3888T>G
|
XP_006711978.1:p.Asn1296Lys
|
|
|
XM_011532473.1:c.3891T>G
|
XP_011530775.1:p.Asn1297Lys
|
|
|
XM_011532474.1:c.3966T>G
|
XP_011530776.1:p.Asn1322Lys
|
|
|
XM_017003117.1:c.3813T>G
|
XP_016858606.1:p.Asn1271Lys
|
|
|
XR_002958896.1:n.4008T>G
|
|
|
|
NM_133259.4:c.3966T>G
MANE Select
|
NP_573566.2:p.Asn1322Lys
|
|
