ENST00000251810.8:c.974A>T
MANE Select
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ENSP00000251810.3:p.Glu325Val
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ENST00000251810.7:c.974A>T
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ENSP00000251810.3:p.Glu325Val
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ENST00000395910.6:n.361A>T
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|
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ENST00000395912.6:c.818A>T
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ENSP00000379248.2:p.Glu273Val
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ENST00000519317.5:c.338A>T
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ENSP00000430641.1:p.Glu113Val
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ENST00000519962.5:c.119A>T
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ENSP00000429140.1:p.Glu40Val
|
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ENST00000522368.5:c.1143A>T
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|
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ENST00000522394.1:c.307A>T
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ENSP00000429578.1:n.307A>T
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ENST00000621845.1:c.812A>T
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ENSP00000484318.1:p.Glu271Val
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NM_001172477.1:c.1190A>T , LRG_788t1:c.1190A>T
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NP_001165948.1:p.Glu397Val
|
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NM_001172478.1:c.818A>T
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NP_001165949.1:p.Glu273Val
|
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NM_015713.4:c.974A>T , LRG_788t2:c.974A>T
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NP_056528.2:p.Glu325Val
|
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NM_001172478.2:c.818A>T
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NP_001165949.1:p.Glu273Val
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NM_015713.5:c.974A>T
MANE Select
|
NP_056528.2:p.Glu325Val
|
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