ENST00000261769.10:c.2298C>A
MANE Select
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ENSP00000261769.4:p.Asp766Glu
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ENST00000261769.9:c.2298C>A
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ENSP00000261769.4:p.Asp766Glu
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ENST00000422392.6:c.2115C>A
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ENSP00000414946.2:p.Asp705Glu
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ENST00000562118.1:n.516C>A
|
|
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ENST00000562836.5:n.2369C>A
|
|
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ENST00000566510.5:c.*964C>A
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ENSP00000458139.1:n.*964C>A
|
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ENST00000566612.5:c.*538C>A
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ENSP00000454782.1:n.*538C>A
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ENST00000611625.4:c.2361C>A
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ENSP00000481063.1:p.Asp787Glu
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ENST00000612417.4:c.1853+3102C>A
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ENSP00000478360.1:n.1853+3102C>A
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ENST00000621016.4:c.1866-4547C>A
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ENSP00000480664.1:n.1866-4547C>A
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NM_004360.3:c.2298C>A , LRG_301t1:c.2298C>A
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NP_004351.1:p.Asp766Glu
|
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XM_011523488.1:c.1563C>A
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XP_011521790.1:p.Asp521Glu
|
|
XM_011523489.1:c.1563C>A
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XP_011521791.1:p.Asp521Glu
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NM_001317184.1:c.2115C>A
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NP_001304113.1:p.Asp705Glu
|
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NM_001317185.1:c.750C>A
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NP_001304114.1:p.Asp250Glu
|
|
NM_001317186.1:c.333C>A
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NP_001304115.1:p.Asp111Glu
|
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NM_004360.4:c.2298C>A
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NP_004351.1:p.Asp766Glu
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NM_004360.5:c.2298C>A
MANE Select
|
NP_004351.1:p.Asp766Glu
|
|
NM_001317184.2:c.2115C>A
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NP_001304113.1:p.Asp705Glu
|
|
NM_001317185.2:c.750C>A
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NP_001304114.1:p.Asp250Glu
|
|
NM_001317186.2:c.333C>A
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NP_001304115.1:p.Asp111Glu
|
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