ENST00000251810.8:c.968T>C
MANE Select
|
ENSP00000251810.3:p.Phe323Ser
|
|
ENST00000251810.7:c.968T>C
|
ENSP00000251810.3:p.Phe323Ser
|
|
ENST00000395910.6:n.355T>C
|
|
|
ENST00000395912.6:c.812T>C
|
ENSP00000379248.2:p.Phe271Ser
|
|
ENST00000519317.5:c.332T>C
|
ENSP00000430641.1:p.Phe111Ser
|
|
ENST00000519962.5:c.113T>C
|
ENSP00000429140.1:p.Phe38Ser
|
|
ENST00000522368.5:c.1137T>C
|
|
|
ENST00000522394.1:c.301T>C
|
ENSP00000429578.1:n.301T>C
|
|
ENST00000621845.1:c.806T>C
|
ENSP00000484318.1:p.Phe269Ser
|
|
NM_001172477.1:c.1184T>C , LRG_788t1:c.1184T>C
|
NP_001165948.1:p.Phe395Ser
|
|
NM_001172478.1:c.812T>C
|
NP_001165949.1:p.Phe271Ser
|
|
NM_015713.4:c.968T>C , LRG_788t2:c.968T>C
|
NP_056528.2:p.Phe323Ser
|
|
NM_001172478.2:c.812T>C
|
NP_001165949.1:p.Phe271Ser
|
|
NM_015713.5:c.968T>C
MANE Select
|
NP_056528.2:p.Phe323Ser
|
|