ENST00000251810.8:c.1027A>C
MANE Select
|
ENSP00000251810.3:p.Asn343His
|
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ENST00000251810.7:c.1027A>C
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ENSP00000251810.3:p.Asn343His
|
|
ENST00000395910.6:n.414A>C
|
|
|
ENST00000395912.6:c.871A>C
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ENSP00000379248.2:p.Asn291His
|
|
ENST00000519317.5:c.391A>C
|
ENSP00000430641.1:p.Asn131His
|
|
ENST00000519962.5:c.172A>C
|
ENSP00000429140.1:p.Asn58His
|
|
ENST00000522368.5:c.1196A>C
|
|
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ENST00000522394.1:c.360A>C
|
ENSP00000429578.1:n.360A>C
|
|
ENST00000621845.1:c.865A>C
|
ENSP00000484318.1:p.Asn289His
|
|
NM_001172477.1:c.1243A>C , LRG_788t1:c.1243A>C
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NP_001165948.1:p.Asn415His
|
|
NM_001172478.1:c.871A>C
|
NP_001165949.1:p.Asn291His
|
|
NM_015713.4:c.1027A>C , LRG_788t2:c.1027A>C
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NP_056528.2:p.Asn343His
|
|
NM_001172478.2:c.871A>C
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NP_001165949.1:p.Asn291His
|
|
NM_015713.5:c.1027A>C
MANE Select
|
NP_056528.2:p.Asn343His
|
|