|
ENST00000409659.6:c.2347G=
|
ENSP00000386562.2:p.Asp783=
|
|
|
ENST00000447246.2:c.2347G=
|
ENSP00000403637.2:p.Asp783=
|
|
|
ENST00000681961.1:n.2367G=
|
|
|
|
ENST00000682104.1:c.2221G=
|
ENSP00000507716.1:p.Asp741=
|
|
|
ENST00000682303.1:c.*2133G=
|
ENSP00000508325.1:n.*2133G=
|
|
|
ENST00000682308.1:c.2347G=
|
ENSP00000507056.1:p.Asp783=
|
|
|
ENST00000682480.1:c.2347G=
|
ENSP00000508344.1:p.Asp783=
|
|
|
ENST00000682546.1:c.2344G=
|
ENSP00000508188.1:p.Asp782=
|
|
|
ENST00000682585.1:c.2347G=
|
ENSP00000506885.1:p.Asp783=
|
|
|
ENST00000682595.1:n.2929G=
|
|
|
|
ENST00000682607.1:c.765G=
|
|
|
|
ENST00000682779.1:c.2338G=
|
ENSP00000507947.1:p.Asp780=
|
|
|
ENST00000682845.1:n.1449G=
|
|
|
|
ENST00000682885.1:c.2302G=
|
ENSP00000508036.1:p.Asp768=
|
|
|
ENST00000682933.1:n.2421G=
|
|
|
|
ENST00000683072.1:n.2929G=
|
|
|
|
ENST00000683125.1:c.2347G=
|
ENSP00000507939.1:p.Asp783=
|
|
|
ENST00000683213.1:c.2350G=
|
ENSP00000507751.1:p.Asp784=
|
|
|
ENST00000683220.1:c.2377G=
|
ENSP00000507151.1:p.Asp793=
|
|
|
ENST00000683329.1:n.3150G=
|
|
|
|
ENST00000683346.1:c.*2222G=
|
ENSP00000507458.1:n.*2222G=
|
|
|
ENST00000683459.1:n.2934G=
|
|
|
|
ENST00000683590.1:c.2347G=
|
ENSP00000506820.1:p.Asp783=
|
|
|
ENST00000683623.1:c.2297-43G=
|
ENSP00000507702.1:n.2297-43G=
|
|
|
ENST00000683645.1:n.2898G=
|
|
|
|
ENST00000683694.1:n.1098G=
|
|
|
|
ENST00000683796.1:c.*2219G=
|
ENSP00000508221.1:n.*2219G=
|
|
|
ENST00000683802.1:n.5272G=
|
|
|
|
ENST00000683833.1:c.2338G=
|
ENSP00000506852.1:p.Asp780=
|
|
|
ENST00000683989.1:c.2347G=
|
ENSP00000507510.1:p.Asp783=
|
|
|
ENST00000683994.1:c.2347G=
|
ENSP00000507181.1:p.Asp783=
|
|
|
ENST00000684290.1:c.*41G=
|
ENSP00000507243.1:n.*41G=
|
|
|
ENST00000684306.1:c.*2260G=
|
ENSP00000508384.1:n.*2260G=
|
|
|
ENST00000684341.1:n.2367G=
|
|
|
|
ENST00000684383.1:c.*1985G=
|
ENSP00000506863.1:n.*1985G=
|
|
|
ENST00000684397.1:c.51G=
|
|
|
|
ENST00000684619.1:c.*2219G=
|
ENSP00000508088.1:n.*2219G=
|
|
|
ENST00000684743.1:n.3378G=
|
|
|
|
ENST00000260665.12:c.2347G=
MANE Select
|
ENSP00000260665.7:p.Asp783=
|
|
|
ENST00000260665.11:c.2347G=
|
ENSP00000260665.7:p.Asp783=
|
|
|
NM_133259.3:c.2347G=
|
NP_573566.2:p.Asp783=
|
|
|
XM_006711915.2:c.2269G=
|
XP_006711978.1:p.Asp757=
|
|
|
XM_006711916.2:c.2347G=
|
XP_006711979.1:p.Asp783=
|
|
|
XM_011532473.1:c.2347G=
|
XP_011530775.1:p.Asp783=
|
|
|
XM_011532474.1:c.2347G=
|
XP_011530776.1:p.Asp783=
|
|
|
XM_006711916.3:c.2347G=
|
XP_006711979.1:p.Asp783=
|
|
|
XM_017003117.1:c.2269G=
|
XP_016858606.1:p.Asp757=
|
|
|
XR_002958896.1:n.2389G=
|
|
|
|
NM_133259.4:c.2347G=
MANE Select
|
NP_573566.2:p.Asp783=
|
|
