ENST00000419884.6:c.236G=
|
|
|
ENST00000472420.6:n.884G=
|
|
|
ENST00000483489.2:n.236G=
|
|
|
ENST00000681993.1:n.1357G=
|
|
|
ENST00000682303.1:c.*3591G=
|
ENSP00000508325.1:n.*3591G=
|
|
ENST00000682308.1:c.3805G=
|
ENSP00000507056.1:p.Asp1269=
|
|
ENST00000682434.1:n.1356G=
|
|
|
ENST00000682480.1:c.3823G=
|
ENSP00000508344.1:p.Asp1275=
|
|
ENST00000682546.1:c.3802G=
|
ENSP00000508188.1:p.Asp1268=
|
|
ENST00000682585.1:c.3805G=
|
ENSP00000506885.1:p.Asp1269=
|
|
ENST00000682595.1:n.4389G=
|
|
|
ENST00000682607.1:c.2223G=
|
|
|
ENST00000682612.1:c.657G=
|
|
|
ENST00000682779.1:c.3796G=
|
ENSP00000507947.1:p.Asp1266=
|
|
ENST00000682885.1:c.3760G=
|
ENSP00000508036.1:p.Asp1254=
|
|
ENST00000682933.1:n.3879G=
|
|
|
ENST00000683002.1:c.657G=
|
|
|
ENST00000683072.1:n.4389G=
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|
|
ENST00000683080.1:n.1424G=
|
|
|
ENST00000683125.1:c.3913G=
|
ENSP00000507939.1:p.Asp1305=
|
|
ENST00000683213.1:c.3808G=
|
ENSP00000507751.1:p.Asp1270=
|
|
ENST00000683220.1:c.3835G=
|
ENSP00000507151.1:p.Asp1279=
|
|
ENST00000683329.1:n.4608G=
|
|
|
ENST00000683346.1:c.*3680G=
|
ENSP00000507458.1:n.*3680G=
|
|
ENST00000683409.1:n.2412G=
|
|
|
ENST00000683459.1:n.4392G=
|
|
|
ENST00000683528.1:c.733G=
|
|
|
ENST00000683590.1:c.3553G=
|
ENSP00000506820.1:p.Asp1185=
|
|
ENST00000683623.1:c.3712G=
|
ENSP00000507702.1:p.Asp1238=
|
|
ENST00000683645.1:n.4356G=
|
|
|
ENST00000683796.1:c.*3677G=
|
ENSP00000508221.1:n.*3677G=
|
|
ENST00000683802.1:n.6730G=
|
|
|
ENST00000683833.1:c.3796G=
|
ENSP00000506852.1:p.Asp1266=
|
|
ENST00000683994.1:c.3805G=
|
ENSP00000507181.1:p.Asp1269=
|
|
ENST00000684290.1:c.*1341G=
|
ENSP00000507243.1:n.*1341G=
|
|
ENST00000684306.1:c.*3718G=
|
ENSP00000508384.1:n.*3718G=
|
|
ENST00000684341.1:n.3825G=
|
|
|
ENST00000684383.1:c.*3443G=
|
ENSP00000506863.1:n.*3443G=
|
|
ENST00000684418.1:n.4986G=
|
|
|
ENST00000684433.1:n.189G=
|
|
|
ENST00000684454.1:n.3155G=
|
|
|
ENST00000684619.1:c.*3677G=
|
ENSP00000508088.1:n.*3677G=
|
|
ENST00000684743.1:n.6550G=
|
|
|
ENST00000260665.12:c.3805G=
MANE Select
|
ENSP00000260665.7:p.Asp1269=
|
|
ENST00000260665.11:c.3805G=
|
ENSP00000260665.7:p.Asp1269=
|
|
ENST00000419884.5:c.46G=
|
ENSP00000414207.1:p.Asp16=
|
|
ENST00000463456.5:n.2848G=
|
|
|
ENST00000472420.5:n.202G=
|
|
|
ENST00000483489.1:n.279G=
|
|
|
NM_133259.3:c.3805G=
|
NP_573566.2:p.Asp1269=
|
|
XM_006711915.2:c.3727G=
|
XP_006711978.1:p.Asp1243=
|
|
XM_011532473.1:c.3805G=
|
XP_011530775.1:p.Asp1269=
|
|
XM_011532474.1:c.3805G=
|
XP_011530776.1:p.Asp1269=
|
|
XM_017003117.1:c.3727G=
|
XP_016858606.1:p.Asp1243=
|
|
XR_002958896.1:n.3847G=
|
|
|
NM_133259.4:c.3805G=
MANE Select
|
NP_573566.2:p.Asp1269=
|
|