ENST00000361510.8:c.2517A>G
MANE Select
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ENSP00000355324.2:p.Glu839=
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ENST00000361828.7:c.2352A>G
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ENSP00000354429.3:p.Glu784=
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ENST00000361908.8:c.2463A>G
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ENSP00000354681.3:p.Glu821=
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ENST00000392436.7:c.2352A>G
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ENSP00000376231.3:p.Glu784=
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ENST00000392437.6:c.2406A>G
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ENSP00000376232.2:p.Glu802=
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ENST00000642289.1:c.2291A>G
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ENST00000642445.1:c.2352A>G
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ENSP00000495535.1:p.Glu784=
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ENST00000642593.1:c.*577A>G
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ENSP00000494273.1:n.*577A>G
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ENST00000643329.1:c.2034A>G
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ENSP00000493673.1:p.Glu678=
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ENST00000643737.1:c.*2433A>G
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ENSP00000494210.1:n.*2433A>G
|
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ENST00000644595.1:c.2352A>G
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ENSP00000494121.1:p.Glu784=
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ENST00000644629.1:c.1939A>G
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ENST00000644841.1:c.*836A>G
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ENSP00000493988.1:n.*836A>G
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ENST00000644959.1:c.2346A>G
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ENST00000645553.1:c.2367A>G
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ENSP00000494725.1:p.Glu789=
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ENST00000646085.1:c.*1830A>G
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ENSP00000494509.1:n.*1830A>G
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ENST00000646277.1:c.*953A>G
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ENSP00000495289.1:n.*953A>G
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ENST00000646544.1:c.1340A>G
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ENST00000646699.1:c.2291A>G
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ENST00000646793.1:c.2244A>G
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ENSP00000494512.1:p.Glu748=
|
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ENST00000361150.6:c.2355A>G
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ENSP00000354781.2:p.Glu785=
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ENST00000361510.6:c.2517A>G
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ENSP00000355324.2:p.Glu839=
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ENST00000361715.6:c.2409A>G
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ENSP00000355311.2:p.Glu803=
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ENST00000361828.6:c.2406A>G
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ENSP00000354429.2:p.Glu802=
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ENST00000361908.7:c.2463A>G
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ENSP00000354681.3:p.Glu821=
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ENST00000392438.7:c.2352A>G
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ENSP00000376233.3:p.Glu784=
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NM_015560.2:c.2352A>G , LRG_337t1:c.2352A>G
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NP_056375.2:p.Glu784=
|
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NM_130831.2:c.2244A>G
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NP_570844.1:p.Glu748=
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NM_130832.2:c.2298A>G
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NP_570845.1:p.Glu766=
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NM_130833.2:c.2355A>G
|
NP_570846.1:p.Glu785=
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NM_130834.2:c.2406A>G
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NP_570847.2:p.Glu802=
|
|
NM_130835.2:c.2409A>G
|
NP_570848.1:p.Glu803=
|
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NM_130836.2:c.2463A>G
|
NP_570849.2:p.Glu821=
|
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NM_130837.2:c.2517A>G , LRG_337t2:c.2517A>G
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NP_570850.2:p.Glu839=
|
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XM_011512863.1:c.2517A>G
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XP_011511165.1:p.Glu839=
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XM_011512864.1:c.2463A>G
|
XP_011511166.1:p.Glu821=
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XM_011512865.1:c.2406A>G
|
XP_011511167.1:p.Glu802=
|
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XM_011512866.1:c.2355A>G
|
XP_011511168.1:p.Glu785=
|
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XM_011512867.1:c.2352A>G
|
XP_011511169.1:p.Glu784=
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XM_011512868.1:c.2244A>G
|
XP_011511170.1:p.Glu748=
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|
XR_924835.1:n.582+9362T>C
|
|
|
NM_001354663.1:c.1983A>G
|
NP_001341592.1:p.Glu661=
|
|
NM_001354664.1:c.1980A>G
|
NP_001341593.1:p.Glu660=
|
|
XR_001740158.2:n.2771A>G
|
|
|
XR_001740159.2:n.2606A>G
|
|
|
XR_001741074.1:n.475+11250T>C
|
|
|
XR_924835.2:n.600+9362T>C
|
|
|
NM_001354663.2:c.1983A>G
|
NP_001341592.1:p.Glu661=
|
|
NM_001354664.2:c.1980A>G
|
NP_001341593.1:p.Glu660=
|
|
NM_130831.3:c.2244A>G
|
NP_570844.1:p.Glu748=
|
|
NM_130832.3:c.2298A>G
|
NP_570845.1:p.Glu766=
|
|
NM_130834.3:c.2406A>G
|
NP_570847.2:p.Glu802=
|
|
NM_130836.3:c.2463A>G
|
NP_570849.2:p.Glu821=
|
|
NM_015560.3:c.2352A>G
|
NP_056375.2:p.Glu784=
|
|
NM_130833.3:c.2355A>G
|
NP_570846.1:p.Glu785=
|
|
NM_130835.3:c.2409A>G
|
NP_570848.1:p.Glu803=
|
|
NM_130837.3:c.2517A>G
MANE Select
|
NP_570850.2:p.Glu839=
|
|