ENST00000681993.1:n.478G=
|
|
|
ENST00000682295.1:c.190G=
|
ENSP00000507499.1:p.Ala64=
|
|
ENST00000682303.1:c.*2712G=
|
ENSP00000508325.1:n.*2712G=
|
|
ENST00000682308.1:c.2926G=
|
ENSP00000507056.1:p.Ala976=
|
|
ENST00000682480.1:c.2926G=
|
ENSP00000508344.1:p.Ala976=
|
|
ENST00000682546.1:c.2923G=
|
ENSP00000508188.1:p.Ala975=
|
|
ENST00000682585.1:c.2926G=
|
ENSP00000506885.1:p.Ala976=
|
|
ENST00000682595.1:n.3510G=
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|
|
ENST00000682607.1:c.1344G=
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|
|
ENST00000682779.1:c.2917G=
|
ENSP00000507947.1:p.Ala973=
|
|
ENST00000682845.1:n.2028G=
|
|
|
ENST00000682885.1:c.2881G=
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ENSP00000508036.1:p.Ala961=
|
|
ENST00000682933.1:n.3000G=
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|
|
ENST00000683072.1:n.3510G=
|
|
|
ENST00000683080.1:n.545G=
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|
|
ENST00000683125.1:c.3034G=
|
ENSP00000507939.1:p.Ala1012=
|
|
ENST00000683213.1:c.2929G=
|
ENSP00000507751.1:p.Ala977=
|
|
ENST00000683220.1:c.2956G=
|
ENSP00000507151.1:p.Ala986=
|
|
ENST00000683236.1:c.256G=
|
ENSP00000506891.1:n.256G=
|
|
ENST00000683329.1:n.3729G=
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|
|
ENST00000683346.1:c.*2801G=
|
ENSP00000507458.1:n.*2801G=
|
|
ENST00000683409.1:n.1533G=
|
|
|
ENST00000683459.1:n.3513G=
|
|
|
ENST00000683590.1:c.2897-5811G=
|
ENSP00000506820.1:n.2897-5811G=
|
|
ENST00000683623.1:c.2833G=
|
ENSP00000507702.1:p.Ala945=
|
|
ENST00000683645.1:n.3477G=
|
|
|
ENST00000683796.1:c.*2798G=
|
ENSP00000508221.1:n.*2798G=
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|
ENST00000683802.1:n.5851G=
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|
|
ENST00000683833.1:c.2917G=
|
ENSP00000506852.1:p.Ala973=
|
|
ENST00000683994.1:c.2926G=
|
ENSP00000507181.1:p.Ala976=
|
|
ENST00000684290.1:c.*462G=
|
ENSP00000507243.1:n.*462G=
|
|
ENST00000684306.1:c.*2839G=
|
ENSP00000508384.1:n.*2839G=
|
|
ENST00000684341.1:n.2946G=
|
|
|
ENST00000684383.1:c.*2564G=
|
ENSP00000506863.1:n.*2564G=
|
|
ENST00000684619.1:c.*2798G=
|
ENSP00000508088.1:n.*2798G=
|
|
ENST00000684705.1:n.47G=
|
|
|
ENST00000684743.1:n.3957G=
|
|
|
ENST00000260665.12:c.2926G=
MANE Select
|
ENSP00000260665.7:p.Ala976=
|
|
ENST00000260665.11:c.2926G=
|
ENSP00000260665.7:p.Ala976=
|
|
NM_133259.3:c.2926G=
|
NP_573566.2:p.Ala976=
|
|
XM_006711915.2:c.2848G=
|
XP_006711978.1:p.Ala950=
|
|
XM_006711916.2:c.2926G=
|
XP_006711979.1:p.Ala976=
|
|
XM_011532473.1:c.2926G=
|
XP_011530775.1:p.Ala976=
|
|
XM_011532474.1:c.2926G=
|
XP_011530776.1:p.Ala976=
|
|
XM_006711916.3:c.2926G=
|
XP_006711979.1:p.Ala976=
|
|
XM_017003117.1:c.2848G=
|
XP_016858606.1:p.Ala950=
|
|
XR_002958896.1:n.2968G=
|
|
|
NM_133259.4:c.2926G=
MANE Select
|
NP_573566.2:p.Ala976=
|
|