ENST00000251810.8:c.1033T>G
MANE Select
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ENSP00000251810.3:p.Phe345Val
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ENST00000251810.7:c.1033T>G
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ENSP00000251810.3:p.Phe345Val
|
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ENST00000395910.6:n.420T>G
|
|
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ENST00000395912.6:c.877T>G
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ENSP00000379248.2:p.Phe293Val
|
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ENST00000519317.5:c.397T>G
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ENSP00000430641.1:p.Phe133Val
|
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ENST00000519962.5:c.178T>G
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ENSP00000429140.1:p.Phe60Val
|
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ENST00000522368.5:c.1202T>G
|
|
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ENST00000522394.1:c.366T>G
|
ENSP00000429578.1:n.366T>G
|
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ENST00000621845.1:c.871T>G
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ENSP00000484318.1:p.Phe291Val
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NM_001172477.1:c.1249T>G , LRG_788t1:c.1249T>G
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NP_001165948.1:p.Phe417Val
|
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NM_001172478.1:c.877T>G
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NP_001165949.1:p.Phe293Val
|
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NM_015713.4:c.1033T>G , LRG_788t2:c.1033T>G
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NP_056528.2:p.Phe345Val
|
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NM_001172478.2:c.877T>G
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NP_001165949.1:p.Phe293Val
|
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NM_015713.5:c.1033T>G
MANE Select
|
NP_056528.2:p.Phe345Val
|
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