ENST00000324856.13:c.5319A>T
MANE Select
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ENSP00000320485.7:p.Leu1773=
|
|
ENST00000374152.7:c.4170A>T
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ENSP00000363267.2:p.Leu1390=
|
|
ENST00000430799.7:c.4167A>T
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ENSP00000390317.3:p.Leu1389=
|
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ENST00000466382.2:c.736A>T
|
|
|
ENST00000636219.1:c.4173A>T
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ENSP00000489842.1:p.Leu1391=
|
|
ENST00000637788.1:n.1119A>T
|
|
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ENST00000324856.11:c.5319A>T
|
ENSP00000320485.7:p.Leu1773=
|
|
ENST00000374152.6:c.4170A>T
|
ENSP00000363267.2:p.Leu1390=
|
|
ENST00000430799.6:c.2008A>T
|
|
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ENST00000457599.6:c.4668A>T
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ENSP00000387636.2:p.Leu1556=
|
|
ENST00000466382.1:c.736A>T
|
|
|
ENST00000532781.1:c.817A>T
|
|
|
NM_006015.4:c.5319A>T , LRG_875t1:c.5319A>T
|
NP_006006.3:p.Leu1773=
|
|
NM_139135.2:c.4668A>T
|
NP_624361.1:p.Leu1556=
|
|
NM_006015.5:c.5319A>T
|
NP_006006.3:p.Leu1773=
|
|
NM_139135.3:c.4668A>T
|
NP_624361.1:p.Leu1556=
|
|
NM_006015.6:c.5319A>T
MANE Select
|
NP_006006.3:p.Leu1773=
|
|
NM_139135.4:c.4668A>T
|
NP_624361.1:p.Leu1556=
|
|