ENST00000251810.8:c.1034T>A
MANE Select
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ENSP00000251810.3:p.Phe345Tyr
|
|
ENST00000251810.7:c.1034T>A
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ENSP00000251810.3:p.Phe345Tyr
|
|
ENST00000395910.6:n.421T>A
|
|
|
ENST00000395912.6:c.878T>A
|
ENSP00000379248.2:p.Phe293Tyr
|
|
ENST00000519317.5:c.398T>A
|
ENSP00000430641.1:p.Phe133Tyr
|
|
ENST00000519962.5:c.179T>A
|
ENSP00000429140.1:p.Phe60Tyr
|
|
ENST00000522368.5:c.1203T>A
|
|
|
ENST00000522394.1:c.367T>A
|
ENSP00000429578.1:n.367T>A
|
|
ENST00000621845.1:c.872T>A
|
ENSP00000484318.1:p.Phe291Tyr
|
|
NM_001172477.1:c.1250T>A , LRG_788t1:c.1250T>A
|
NP_001165948.1:p.Phe417Tyr
|
|
NM_001172478.1:c.878T>A
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NP_001165949.1:p.Phe293Tyr
|
|
NM_015713.4:c.1034T>A , LRG_788t2:c.1034T>A
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NP_056528.2:p.Phe345Tyr
|
|
NM_001172478.2:c.878T>A
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NP_001165949.1:p.Phe293Tyr
|
|
NM_015713.5:c.1034T>A
MANE Select
|
NP_056528.2:p.Phe345Tyr
|
|