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ENST00000506007.2:n.2962G=
|
|
|
|
ENST00000513232.2:c.*1387G=
|
ENSP00000422749.2:n.*1387G=
|
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ENST00000698450.1:n.1891G=
|
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ENST00000698451.1:n.2092G=
|
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ENST00000698452.1:n.3163G=
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ENST00000698453.1:c.2442-94G=
|
ENSP00000513735.1:n.2442-94G=
|
|
|
ENST00000698454.1:c.2498G=
|
ENSP00000513736.1:p.Cys833=
|
|
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ENST00000698455.1:c.*2648G=
|
ENSP00000513737.1:n.*2648G=
|
|
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ENST00000698456.1:c.*1365G=
|
ENSP00000513738.1:n.*1365G=
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|
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ENST00000698457.1:c.2297G=
|
ENSP00000513739.1:p.Cys766=
|
|
|
ENST00000698458.1:c.2478-94G=
|
ENSP00000513740.1:n.2478-94G=
|
|
|
ENST00000698459.1:c.2507G=
|
ENSP00000513741.1:p.Cys836=
|
|
|
ENST00000698460.1:c.*279-94G=
|
ENSP00000513742.1:n.*279-94G=
|
|
|
ENST00000698461.1:n.2962G=
|
|
|
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ENST00000698462.1:n.2882G=
|
|
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ENST00000698468.1:n.3163G=
|
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ENST00000698469.1:c.*2019G=
|
ENSP00000513743.1:n.*2019G=
|
|
|
ENST00000698470.1:c.*514G=
|
ENSP00000513744.1:n.*514G=
|
|
|
ENST00000698471.1:n.2962G=
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|
|
|
ENST00000698472.1:c.*1387G=
|
ENSP00000513745.1:n.*1387G=
|
|
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ENST00000698473.1:n.2962G=
|
|
|
|
ENST00000698474.1:n.2962G=
|
|
|
|
ENST00000698475.1:n.3047G=
|
|
|
|
ENST00000698476.1:c.2507G=
|
ENSP00000513746.1:p.Cys836=
|
|
|
ENST00000698477.1:c.2442-94G=
|
ENSP00000513747.1:n.2442-94G=
|
|
|
ENST00000698478.1:n.2962G=
|
|
|
|
ENST00000698479.1:c.2507G=
|
ENSP00000513748.1:p.Cys836=
|
|
|
ENST00000698480.1:c.2437-94G=
|
ENSP00000513749.1:n.2437-94G=
|
|
|
ENST00000698481.1:c.2437-94G=
|
ENSP00000513750.1:n.2437-94G=
|
|
|
ENST00000698482.1:n.2797G=
|
|
|
|
ENST00000698483.1:n.2962G=
|
|
|
|
ENST00000698484.1:c.2507G=
|
ENSP00000513751.1:p.Cys836=
|
|
|
ENST00000698485.1:c.2437-94G=
|
ENSP00000513752.1:n.2437-94G=
|
|
|
ENST00000698486.1:n.2962G=
|
|
|
|
ENST00000698487.1:c.2507G=
|
ENSP00000513753.1:p.Cys836=
|
|
|
ENST00000698488.1:c.2260-94G=
|
ENSP00000513754.1:n.2260-94G=
|
|
|
ENST00000698489.1:n.6747G=
|
|
|
|
ENST00000698490.1:c.2507G=
|
ENSP00000513755.1:p.Cys836=
|
|
|
ENST00000698492.1:c.*1222G=
|
ENSP00000513756.1:n.*1222G=
|
|
|
ENST00000698493.1:n.2797G=
|
|
|
|
ENST00000698494.1:c.*402G=
|
ENSP00000513757.1:n.*402G=
|
|
|
ENST00000358746.7:c.2507G=
MANE Select
|
ENSP00000351596.3:p.Cys836=
|
|
|
ENST00000649566.1:c.2507G=
|
ENSP00000497948.1:p.Cys836=
|
|
|
ENST00000358746.6:c.2507G=
|
ENSP00000351596.2:p.Cys836=
|
|
|
ENST00000506007.1:n.89G=
|
|
|
|
ENST00000507805.5:n.694G=
|
|
|
|
NM_014639.3:c.2507G= , LRG_173t1:c.2507G=
|
NP_055454.1:p.Cys836=
|
|
|
XR_948312.1:n.2776G=
|
|
|
|
XR_001742370.2:n.2779G=
|
|
|
|
NM_014639.4:c.2507G=
MANE Select
|
NP_055454.1:p.Cys836=
|
|
