ENST00000251810.8:c.1049A>T
MANE Select
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ENSP00000251810.3:p.Asp350Val
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ENST00000251810.7:c.1049A>T
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ENSP00000251810.3:p.Asp350Val
|
|
ENST00000395910.6:n.436A>T
|
|
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ENST00000395912.6:c.893A>T
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ENSP00000379248.2:p.Asp298Val
|
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ENST00000519317.5:c.413A>T
|
ENSP00000430641.1:p.Asp138Val
|
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ENST00000519962.5:c.194A>T
|
ENSP00000429140.1:p.Asp65Val
|
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ENST00000522368.5:c.1218A>T
|
|
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ENST00000522394.1:c.382A>T
|
ENSP00000429578.1:n.382A>T
|
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ENST00000621845.1:c.887A>T
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ENSP00000484318.1:p.Asp296Val
|
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NM_001172477.1:c.1265A>T , LRG_788t1:c.1265A>T
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NP_001165948.1:p.Asp422Val
|
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NM_001172478.1:c.893A>T
|
NP_001165949.1:p.Asp298Val
|
|
NM_015713.4:c.1049A>T , LRG_788t2:c.1049A>T
|
NP_056528.2:p.Asp350Val
|
|
NM_001172478.2:c.893A>T
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NP_001165949.1:p.Asp298Val
|
|
NM_015713.5:c.1049A>T
MANE Select
|
NP_056528.2:p.Asp350Val
|
|