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ENST00000681993.1:n.683G=
|
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|
ENST00000682295.1:c.303+214G=
|
ENSP00000507499.1:n.303+214G=
|
|
|
ENST00000682303.1:c.*2917G=
|
ENSP00000508325.1:n.*2917G=
|
|
|
ENST00000682308.1:c.3131G=
|
ENSP00000507056.1:p.Arg1044=
|
|
|
ENST00000682480.1:c.3149G=
|
ENSP00000508344.1:p.Arg1050=
|
|
|
ENST00000682546.1:c.3128G=
|
ENSP00000508188.1:p.Arg1043=
|
|
|
ENST00000682585.1:c.3131G=
|
ENSP00000506885.1:p.Arg1044=
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ENST00000682595.1:n.3715G=
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ENST00000682607.1:c.1549G=
|
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ENST00000682779.1:c.3122G=
|
ENSP00000507947.1:p.Arg1041=
|
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ENST00000682845.1:n.2233G=
|
|
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|
ENST00000682885.1:c.3086G=
|
ENSP00000508036.1:p.Arg1029=
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ENST00000682933.1:n.3205G=
|
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ENST00000683072.1:n.3715G=
|
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ENST00000683080.1:n.750G=
|
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ENST00000683125.1:c.3239G=
|
ENSP00000507939.1:p.Arg1080=
|
|
|
ENST00000683213.1:c.3134G=
|
ENSP00000507751.1:p.Arg1045=
|
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ENST00000683220.1:c.3161G=
|
ENSP00000507151.1:p.Arg1054=
|
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ENST00000683329.1:n.3934G=
|
|
|
|
ENST00000683346.1:c.*3006G=
|
ENSP00000507458.1:n.*3006G=
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ENST00000683409.1:n.1738G=
|
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ENST00000683459.1:n.3718G=
|
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ENST00000683590.1:c.2897-5484G=
|
ENSP00000506820.1:n.2897-5484G=
|
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ENST00000683623.1:c.3038G=
|
ENSP00000507702.1:p.Arg1013=
|
|
|
ENST00000683645.1:n.3682G=
|
|
|
|
ENST00000683796.1:c.*3003G=
|
ENSP00000508221.1:n.*3003G=
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ENST00000683802.1:n.6056G=
|
|
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|
ENST00000683833.1:c.3122G=
|
ENSP00000506852.1:p.Arg1041=
|
|
|
ENST00000683994.1:c.3131G=
|
ENSP00000507181.1:p.Arg1044=
|
|
|
ENST00000684290.1:c.*667G=
|
ENSP00000507243.1:n.*667G=
|
|
|
ENST00000684306.1:c.*3044G=
|
ENSP00000508384.1:n.*3044G=
|
|
|
ENST00000684341.1:n.3151G=
|
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|
ENST00000684383.1:c.*2769G=
|
ENSP00000506863.1:n.*2769G=
|
|
|
ENST00000684619.1:c.*3003G=
|
ENSP00000508088.1:n.*3003G=
|
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ENST00000684705.1:n.252G=
|
|
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|
ENST00000684743.1:n.4162G=
|
|
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|
ENST00000260665.12:c.3131G=
MANE Select
|
ENSP00000260665.7:p.Arg1044=
|
|
|
ENST00000260665.11:c.3131G=
|
ENSP00000260665.7:p.Arg1044=
|
|
|
NM_133259.3:c.3131G=
|
NP_573566.2:p.Arg1044=
|
|
|
XM_006711915.2:c.3053G=
|
XP_006711978.1:p.Arg1018=
|
|
|
XM_006711916.2:c.3131G=
|
XP_006711979.1:p.Arg1044=
|
|
|
XM_011532473.1:c.3131G=
|
XP_011530775.1:p.Arg1044=
|
|
|
XM_011532474.1:c.3131G=
|
XP_011530776.1:p.Arg1044=
|
|
|
XM_006711916.3:c.3131G=
|
XP_006711979.1:p.Arg1044=
|
|
|
XM_017003117.1:c.3053G=
|
XP_016858606.1:p.Arg1018=
|
|
|
XR_002958896.1:n.3173G=
|
|
|
|
NM_133259.4:c.3131G=
MANE Select
|
NP_573566.2:p.Arg1044=
|
|
