ENST00000419884.6:c.160A>G
|
|
|
ENST00000472420.6:n.808A>G
|
|
|
ENST00000483489.2:n.160A>G
|
|
|
ENST00000681993.1:n.1281A>G
|
|
|
ENST00000682303.1:c.*3515A>G
|
ENSP00000508325.1:n.*3515A>G
|
|
ENST00000682308.1:c.3729A>G
|
ENSP00000507056.1:p.Arg1243=
|
|
ENST00000682434.1:n.1280A>G
|
|
|
ENST00000682480.1:c.3747A>G
|
ENSP00000508344.1:p.Arg1249=
|
|
ENST00000682546.1:c.3726A>G
|
ENSP00000508188.1:p.Arg1242=
|
|
ENST00000682585.1:c.3729A>G
|
ENSP00000506885.1:p.Arg1243=
|
|
ENST00000682595.1:n.4313A>G
|
|
|
ENST00000682607.1:c.2147A>G
|
|
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ENST00000682612.1:c.581A>G
|
|
|
ENST00000682779.1:c.3720A>G
|
ENSP00000507947.1:p.Arg1240=
|
|
ENST00000682845.1:n.2831A>G
|
|
|
ENST00000682885.1:c.3684A>G
|
ENSP00000508036.1:p.Arg1228=
|
|
ENST00000682933.1:n.3803A>G
|
|
|
ENST00000683002.1:c.581A>G
|
|
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ENST00000683072.1:n.4313A>G
|
|
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ENST00000683080.1:n.1348A>G
|
|
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ENST00000683125.1:c.3837A>G
|
ENSP00000507939.1:p.Arg1279=
|
|
ENST00000683213.1:c.3732A>G
|
ENSP00000507751.1:p.Arg1244=
|
|
ENST00000683220.1:c.3759A>G
|
ENSP00000507151.1:p.Arg1253=
|
|
ENST00000683329.1:n.4532A>G
|
|
|
ENST00000683346.1:c.*3604A>G
|
ENSP00000507458.1:n.*3604A>G
|
|
ENST00000683409.1:n.2336A>G
|
|
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ENST00000683459.1:n.4316A>G
|
|
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ENST00000683528.1:c.657A>G
|
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ENST00000683590.1:c.3477A>G
|
ENSP00000506820.1:p.Arg1159=
|
|
ENST00000683623.1:c.3636A>G
|
ENSP00000507702.1:p.Arg1212=
|
|
ENST00000683645.1:n.4280A>G
|
|
|
ENST00000683796.1:c.*3601A>G
|
ENSP00000508221.1:n.*3601A>G
|
|
ENST00000683802.1:n.6654A>G
|
|
|
ENST00000683833.1:c.3720A>G
|
ENSP00000506852.1:p.Arg1240=
|
|
ENST00000683994.1:c.3729A>G
|
ENSP00000507181.1:p.Arg1243=
|
|
ENST00000684290.1:c.*1265A>G
|
ENSP00000507243.1:n.*1265A>G
|
|
ENST00000684306.1:c.*3642A>G
|
ENSP00000508384.1:n.*3642A>G
|
|
ENST00000684341.1:n.3749A>G
|
|
|
ENST00000684383.1:c.*3367A>G
|
ENSP00000506863.1:n.*3367A>G
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ENST00000684418.1:n.4910A>G
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ENST00000684433.1:n.113A>G
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ENST00000684454.1:n.3079A>G
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|
|
ENST00000684619.1:c.*3601A>G
|
ENSP00000508088.1:n.*3601A>G
|
|
ENST00000684743.1:n.6474A>G
|
|
|
ENST00000260665.12:c.3729A>G
MANE Select
|
ENSP00000260665.7:p.Arg1243=
|
|
ENST00000260665.11:c.3729A>G
|
ENSP00000260665.7:p.Arg1243=
|
|
ENST00000463456.5:n.2772A>G
|
|
|
ENST00000472420.5:n.126A>G
|
|
|
ENST00000483489.1:n.203A>G
|
|
|
NM_133259.3:c.3729A>G
|
NP_573566.2:p.Arg1243=
|
|
XM_006711915.2:c.3651A>G
|
XP_006711978.1:p.Arg1217=
|
|
XM_011532473.1:c.3729A>G
|
XP_011530775.1:p.Arg1243=
|
|
XM_011532474.1:c.3729A>G
|
XP_011530776.1:p.Arg1243=
|
|
XM_017003117.1:c.3651A>G
|
XP_016858606.1:p.Arg1217=
|
|
XR_002958896.1:n.3771A>G
|
|
|
NM_133259.4:c.3729A>G
MANE Select
|
NP_573566.2:p.Arg1243=
|
|