ENST00000367435.5:c.977G>A
MANE Select
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ENSP00000356405.4:p.Gly326Asp
|
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ENST00000635846.1:c.734G>A
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ENSP00000490035.1:p.Gly245Asp
|
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ENST00000643006.1:c.1045G>A
|
ENSP00000496633.1:p.Val349Met
|
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ENST00000648071.1:c.*953G>A
|
ENSP00000497513.1:n.*953G>A
|
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ENST00000649613.1:n.227G>A
|
|
|
ENST00000649895.1:n.1195G>A
|
|
|
ENST00000650197.1:c.977G>A
|
ENSP00000496929.1:p.Gly326Asp
|
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ENST00000367435.3:c.977G>A
|
ENSP00000356405.3:p.Gly326Asp
|
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NM_024529.4:c.977G>A , LRG_507t1:c.977G>A
|
NP_078805.3:p.Gly326Asp
|
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NM_024529.5:c.977G>A
MANE Select
|
NP_078805.3:p.Gly326Asp
|
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