ENST00000251810.8:c.970T>A
MANE Select
|
ENSP00000251810.3:p.Phe324Ile
|
|
ENST00000251810.7:c.970T>A
|
ENSP00000251810.3:p.Phe324Ile
|
|
ENST00000395910.6:n.357T>A
|
|
|
ENST00000395912.6:c.814T>A
|
ENSP00000379248.2:p.Phe272Ile
|
|
ENST00000519317.5:c.334T>A
|
ENSP00000430641.1:p.Phe112Ile
|
|
ENST00000519962.5:c.115T>A
|
ENSP00000429140.1:p.Phe39Ile
|
|
ENST00000522368.5:c.1139T>A
|
|
|
ENST00000522394.1:c.303T>A
|
ENSP00000429578.1:n.303T>A
|
|
ENST00000621845.1:c.808T>A
|
ENSP00000484318.1:p.Phe270Ile
|
|
NM_001172477.1:c.1186T>A , LRG_788t1:c.1186T>A
|
NP_001165948.1:p.Phe396Ile
|
|
NM_001172478.1:c.814T>A
|
NP_001165949.1:p.Phe272Ile
|
|
NM_015713.4:c.970T>A , LRG_788t2:c.970T>A
|
NP_056528.2:p.Phe324Ile
|
|
NM_001172478.2:c.814T>A
|
NP_001165949.1:p.Phe272Ile
|
|
NM_015713.5:c.970T>A
MANE Select
|
NP_056528.2:p.Phe324Ile
|
|