ENST00000251810.8:c.1052T>C
MANE Select
|
ENSP00000251810.3:p.Phe351Ser
|
|
ENST00000251810.7:c.1052T>C
|
ENSP00000251810.3:p.Phe351Ser
|
|
ENST00000395910.6:n.439T>C
|
|
|
ENST00000395912.6:c.896T>C
|
ENSP00000379248.2:p.Phe299Ser
|
|
ENST00000519317.5:c.416T>C
|
ENSP00000430641.1:p.Phe139Ser
|
|
ENST00000519962.5:c.197T>C
|
ENSP00000429140.1:p.Phe66Ser
|
|
ENST00000522368.5:c.1221T>C
|
|
|
ENST00000522394.1:c.385T>C
|
ENSP00000429578.1:n.385T>C
|
|
ENST00000621845.1:c.890T>C
|
ENSP00000484318.1:p.Phe297Ser
|
|
NM_001172477.1:c.1268T>C , LRG_788t1:c.1268T>C
|
NP_001165948.1:p.Phe423Ser
|
|
NM_001172478.1:c.896T>C
|
NP_001165949.1:p.Phe299Ser
|
|
NM_015713.4:c.1052T>C , LRG_788t2:c.1052T>C
|
NP_056528.2:p.Phe351Ser
|
|
NM_001172478.2:c.896T>C
|
NP_001165949.1:p.Phe299Ser
|
|
NM_015713.5:c.1052T>C
MANE Select
|
NP_056528.2:p.Phe351Ser
|
|