|
ENST00000409659.6:c.2299G=
|
ENSP00000386562.2:p.Ala767=
|
|
|
ENST00000447246.2:c.2299G=
|
ENSP00000403637.2:p.Ala767=
|
|
|
ENST00000681961.1:n.2319G=
|
|
|
|
ENST00000682104.1:c.2173G=
|
ENSP00000507716.1:p.Ala725=
|
|
|
ENST00000682303.1:c.*2085G=
|
ENSP00000508325.1:n.*2085G=
|
|
|
ENST00000682308.1:c.2299G=
|
ENSP00000507056.1:p.Ala767=
|
|
|
ENST00000682480.1:c.2299G=
|
ENSP00000508344.1:p.Ala767=
|
|
|
ENST00000682546.1:c.2296G=
|
ENSP00000508188.1:p.Ala766=
|
|
|
ENST00000682585.1:c.2299G=
|
ENSP00000506885.1:p.Ala767=
|
|
|
ENST00000682595.1:n.2881G=
|
|
|
|
ENST00000682607.1:c.717G=
|
|
|
|
ENST00000682779.1:c.2290G=
|
ENSP00000507947.1:p.Ala764=
|
|
|
ENST00000682845.1:n.1401G=
|
|
|
|
ENST00000682885.1:c.2254G=
|
ENSP00000508036.1:p.Ala752=
|
|
|
ENST00000682933.1:n.2373G=
|
|
|
|
ENST00000683072.1:n.2881G=
|
|
|
|
ENST00000683125.1:c.2299G=
|
ENSP00000507939.1:p.Ala767=
|
|
|
ENST00000683213.1:c.2302G=
|
ENSP00000507751.1:p.Ala768=
|
|
|
ENST00000683220.1:c.2329G=
|
ENSP00000507151.1:p.Ala777=
|
|
|
ENST00000683329.1:n.3102G=
|
|
|
|
ENST00000683346.1:c.*2174G=
|
ENSP00000507458.1:n.*2174G=
|
|
|
ENST00000683459.1:n.2886G=
|
|
|
|
ENST00000683590.1:c.2299G=
|
ENSP00000506820.1:p.Ala767=
|
|
|
ENST00000683623.1:c.2297-91G=
|
ENSP00000507702.1:n.2297-91G=
|
|
|
ENST00000683645.1:n.2850G=
|
|
|
|
ENST00000683694.1:n.1050G=
|
|
|
|
ENST00000683796.1:c.*2171G=
|
ENSP00000508221.1:n.*2171G=
|
|
|
ENST00000683802.1:n.5224G=
|
|
|
|
ENST00000683833.1:c.2290G=
|
ENSP00000506852.1:p.Ala764=
|
|
|
ENST00000683989.1:c.2299G=
|
ENSP00000507510.1:p.Ala767=
|
|
|
ENST00000683994.1:c.2299G=
|
ENSP00000507181.1:p.Ala767=
|
|
|
ENST00000684290.1:c.2213G=
|
ENSP00000507243.1:p.Cys738=
|
|
|
ENST00000684306.1:c.*2212G=
|
ENSP00000508384.1:n.*2212G=
|
|
|
ENST00000684341.1:n.2319G=
|
|
|
|
ENST00000684383.1:c.*1937G=
|
ENSP00000506863.1:n.*1937G=
|
|
|
ENST00000684397.1:c.3G=
|
|
|
|
ENST00000684619.1:c.*2171G=
|
ENSP00000508088.1:n.*2171G=
|
|
|
ENST00000684743.1:n.3330G=
|
|
|
|
ENST00000260665.12:c.2299G=
MANE Select
|
ENSP00000260665.7:p.Ala767=
|
|
|
ENST00000260665.11:c.2299G=
|
ENSP00000260665.7:p.Ala767=
|
|
|
NM_133259.3:c.2299G=
|
NP_573566.2:p.Ala767=
|
|
|
XM_006711915.2:c.2221G=
|
XP_006711978.1:p.Ala741=
|
|
|
XM_006711916.2:c.2299G=
|
XP_006711979.1:p.Ala767=
|
|
|
XM_011532473.1:c.2299G=
|
XP_011530775.1:p.Ala767=
|
|
|
XM_011532474.1:c.2299G=
|
XP_011530776.1:p.Ala767=
|
|
|
XM_006711916.3:c.2299G=
|
XP_006711979.1:p.Ala767=
|
|
|
XM_017003117.1:c.2221G=
|
XP_016858606.1:p.Ala741=
|
|
|
XR_002958896.1:n.2341G=
|
|
|
|
NM_133259.4:c.2299G=
MANE Select
|
NP_573566.2:p.Ala767=
|
|
