ENST00000261769.10:c.2592A>C
MANE Select
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ENSP00000261769.4:p.Glu864Asp
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ENST00000261769.9:c.2592A>C
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ENSP00000261769.4:p.Glu864Asp
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ENST00000422392.6:c.2409A>C
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ENSP00000414946.2:p.Glu803Asp
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ENST00000562118.1:n.810A>C
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ENST00000562836.5:n.2663A>C
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ENST00000566510.5:c.*1258A>C
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ENSP00000458139.1:n.*1258A>C
|
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ENST00000566612.5:c.*832A>C
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ENSP00000454782.1:n.*832A>C
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ENST00000611625.4:c.2655A>C
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ENSP00000481063.1:p.Glu885Asp
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ENST00000612417.4:c.1854-749A>C
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ENSP00000478360.1:n.1854-749A>C
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ENST00000621016.4:c.1866-761A>C
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ENSP00000480664.1:n.1866-761A>C
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NM_004360.3:c.2592A>C , LRG_301t1:c.2592A>C
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NP_004351.1:p.Glu864Asp
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XM_011523488.1:c.1857A>C
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XP_011521790.1:p.Glu619Asp
|
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XM_011523489.1:c.1857A>C
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XP_011521791.1:p.Glu619Asp
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NM_001317184.1:c.2409A>C
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NP_001304113.1:p.Glu803Asp
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NM_001317185.1:c.1044A>C
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NP_001304114.1:p.Glu348Asp
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NM_001317186.1:c.627A>C
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NP_001304115.1:p.Glu209Asp
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NM_004360.4:c.2592A>C
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NP_004351.1:p.Glu864Asp
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NM_004360.5:c.2592A>C
MANE Select
|
NP_004351.1:p.Glu864Asp
|
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NM_001317184.2:c.2409A>C
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NP_001304113.1:p.Glu803Asp
|
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NM_001317185.2:c.1044A>C
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NP_001304114.1:p.Glu348Asp
|
|
NM_001317186.2:c.627A>C
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NP_001304115.1:p.Glu209Asp
|
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