ENST00000506007.2:n.3070G=
|
|
|
ENST00000513232.2:c.*1495G=
|
ENSP00000422749.2:n.*1495G=
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|
ENST00000698450.1:n.1914G=
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|
|
ENST00000698451.1:n.2200G=
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|
|
ENST00000698452.1:n.3271G=
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|
|
ENST00000698453.1:c.2456G=
|
ENSP00000513735.1:p.Cys819=
|
|
ENST00000698454.1:c.2521G=
|
ENSP00000513736.1:p.Ala841=
|
|
ENST00000698455.1:c.*2756G=
|
ENSP00000513737.1:n.*2756G=
|
|
ENST00000698456.1:c.*1388G=
|
ENSP00000513738.1:n.*1388G=
|
|
ENST00000698457.1:c.2320G=
|
ENSP00000513739.1:p.Ala774=
|
|
ENST00000698458.1:c.2492G=
|
ENSP00000513740.1:p.Cys831=
|
|
ENST00000698459.1:c.2530G=
|
ENSP00000513741.1:p.Ala844=
|
|
ENST00000698460.1:c.*293G=
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ENSP00000513742.1:n.*293G=
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|
ENST00000698461.1:n.2985G=
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|
|
ENST00000698462.1:n.2905G=
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|
|
ENST00000698468.1:n.3271G=
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|
|
ENST00000698469.1:c.*2127G=
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ENSP00000513743.1:n.*2127G=
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|
ENST00000698470.1:c.*622G=
|
ENSP00000513744.1:n.*622G=
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|
ENST00000698471.1:n.3070G=
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|
|
ENST00000698472.1:c.*1495G=
|
ENSP00000513745.1:n.*1495G=
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|
ENST00000698473.1:n.3070G=
|
|
|
ENST00000698474.1:n.3070G=
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|
|
ENST00000698475.1:n.3155G=
|
|
|
ENST00000698476.1:c.2530G=
|
ENSP00000513746.1:p.Ala844=
|
|
ENST00000698477.1:c.2456G=
|
ENSP00000513747.1:p.Cys819=
|
|
ENST00000698478.1:n.3070G=
|
|
|
ENST00000698479.1:c.2530G=
|
ENSP00000513748.1:p.Ala844=
|
|
ENST00000698480.1:c.2451G=
|
ENSP00000513749.1:p.Met817=
|
|
ENST00000698481.1:c.2451G=
|
ENSP00000513750.1:p.Met817=
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|
ENST00000698482.1:n.2820G=
|
|
|
ENST00000698483.1:n.2985G=
|
|
|
ENST00000698484.1:c.2530G=
|
ENSP00000513751.1:p.Ala844=
|
|
ENST00000698485.1:c.2451G=
|
ENSP00000513752.1:p.Met817=
|
|
ENST00000698486.1:n.3070G=
|
|
|
ENST00000698487.1:c.2530G=
|
ENSP00000513753.1:p.Ala844=
|
|
ENST00000698488.1:c.2274G=
|
ENSP00000513754.1:p.Met758=
|
|
ENST00000698489.1:n.6855G=
|
|
|
ENST00000698490.1:c.2530G=
|
ENSP00000513755.1:p.Ala844=
|
|
ENST00000698492.1:c.*1245G=
|
ENSP00000513756.1:n.*1245G=
|
|
ENST00000698493.1:n.2820G=
|
|
|
ENST00000698494.1:c.*510G=
|
ENSP00000513757.1:n.*510G=
|
|
ENST00000358746.7:c.2530G=
MANE Select
|
ENSP00000351596.3:p.Ala844=
|
|
ENST00000649566.1:c.2530G=
|
ENSP00000497948.1:p.Ala844=
|
|
ENST00000358746.6:c.2530G=
|
ENSP00000351596.2:p.Ala844=
|
|
ENST00000506007.1:n.197G=
|
|
|
ENST00000507805.5:n.802G=
|
|
|
ENST00000508181.5:n.103G=
|
|
|
NM_014639.3:c.2530G= , LRG_173t1:c.2530G=
|
NP_055454.1:p.Ala844=
|
|
XR_948312.1:n.2799G=
|
|
|
XR_001742370.2:n.2802G=
|
|
|
NM_014639.4:c.2530G=
MANE Select
|
NP_055454.1:p.Ala844=
|
|