|
ENST00000419884.6:c.570T>G
|
|
|
|
ENST00000681993.1:n.1492T>G
|
|
|
|
ENST00000682154.1:n.1374T>G
|
|
|
|
ENST00000682303.1:c.*3651T>G
|
ENSP00000508325.1:n.*3651T>G
|
|
|
ENST00000682308.1:c.3865T>G
|
ENSP00000507056.1:p.Leu1289Val
|
|
|
ENST00000682434.1:n.3495T>G
|
|
|
|
ENST00000682480.1:c.3958T>G
|
ENSP00000508344.1:p.Leu1320Val
|
|
|
ENST00000682546.1:c.3937T>G
|
ENSP00000508188.1:p.Leu1313Val
|
|
|
ENST00000682585.1:c.*68T>G
|
ENSP00000506885.1:n.*68T>G
|
|
|
ENST00000682607.1:c.2683T>G
|
|
|
|
ENST00000682612.1:c.752+2044T>G
|
|
|
|
ENST00000682696.1:c.40T>G
|
ENSP00000508411.1:p.Leu14Val
|
|
|
ENST00000682779.1:c.3931T>G
|
ENSP00000507947.1:p.Leu1311Val
|
|
|
ENST00000682885.1:c.3895T>G
|
ENSP00000508036.1:p.Leu1299Val
|
|
|
ENST00000682933.1:n.4140T>G
|
|
|
|
ENST00000683002.1:c.792T>G
|
|
|
|
ENST00000683072.1:n.4524T>G
|
|
|
|
ENST00000683080.1:n.1559T>G
|
|
|
|
ENST00000683096.1:n.2381T>G
|
|
|
|
ENST00000683125.1:c.4048T>G
|
ENSP00000507939.1:p.Leu1350Val
|
|
|
ENST00000683213.1:c.3943T>G
|
ENSP00000507751.1:p.Leu1315Val
|
|
|
ENST00000683220.1:c.3970T>G
|
ENSP00000507151.1:p.Leu1324Val
|
|
|
ENST00000683329.1:n.4743T>G
|
|
|
|
ENST00000683346.1:c.*3815T>G
|
ENSP00000507458.1:n.*3815T>G
|
|
|
ENST00000683409.1:n.2472T>G
|
|
|
|
ENST00000683459.1:n.4527T>G
|
|
|
|
ENST00000683590.1:c.3613T>G
|
ENSP00000506820.1:p.Leu1205Val
|
|
|
ENST00000683623.1:c.3847T>G
|
ENSP00000507702.1:p.Leu1283Val
|
|
|
ENST00000683796.1:c.*3737T>G
|
ENSP00000508221.1:n.*3737T>G
|
|
|
ENST00000683833.1:c.3856T>G
|
ENSP00000506852.1:p.Leu1286Val
|
|
|
ENST00000683994.1:c.*53T>G
|
ENSP00000507181.1:n.*53T>G
|
|
|
ENST00000684290.1:c.*1401T>G
|
ENSP00000507243.1:n.*1401T>G
|
|
|
ENST00000684306.1:c.*3853T>G
|
ENSP00000508384.1:n.*3853T>G
|
|
|
ENST00000684383.1:c.*3578T>G
|
ENSP00000506863.1:n.*3578T>G
|
|
|
ENST00000684418.1:n.5121T>G
|
|
|
|
ENST00000684433.1:n.324T>G
|
|
|
|
ENST00000684454.1:n.7804T>G
|
|
|
|
ENST00000684619.1:c.*3812T>G
|
ENSP00000508088.1:n.*3812T>G
|
|
|
ENST00000684743.1:n.6685T>G
|
|
|
|
ENST00000260665.12:c.3940T>G
MANE Select
|
ENSP00000260665.7:p.Leu1314Val
|
|
|
ENST00000260665.11:c.3940T>G
|
ENSP00000260665.7:p.Leu1314Val
|
|
|
ENST00000419884.5:c.181T>G
|
ENSP00000414207.1:p.Leu61Val
|
|
|
ENST00000463456.5:n.2983T>G
|
|
|
|
NM_133259.3:c.3940T>G
|
NP_573566.2:p.Leu1314Val
|
|
|
XM_006711915.2:c.3862T>G
|
XP_006711978.1:p.Leu1288Val
|
|
|
XM_011532473.1:c.3865T>G
|
XP_011530775.1:p.Leu1289Val
|
|
|
XM_011532474.1:c.3940T>G
|
XP_011530776.1:p.Leu1314Val
|
|
|
XM_017003117.1:c.3787T>G
|
XP_016858606.1:p.Leu1263Val
|
|
|
XR_002958896.1:n.3982T>G
|
|
|
|
NM_133259.4:c.3940T>G
MANE Select
|
NP_573566.2:p.Leu1314Val
|
|
