ENST00000251810.8:c.971T>G
MANE Select
|
ENSP00000251810.3:p.Phe324Cys
|
|
ENST00000251810.7:c.971T>G
|
ENSP00000251810.3:p.Phe324Cys
|
|
ENST00000395910.6:n.358T>G
|
|
|
ENST00000395912.6:c.815T>G
|
ENSP00000379248.2:p.Phe272Cys
|
|
ENST00000519317.5:c.335T>G
|
ENSP00000430641.1:p.Phe112Cys
|
|
ENST00000519962.5:c.116T>G
|
ENSP00000429140.1:p.Phe39Cys
|
|
ENST00000522368.5:c.1140T>G
|
|
|
ENST00000522394.1:c.304T>G
|
ENSP00000429578.1:n.304T>G
|
|
ENST00000621845.1:c.809T>G
|
ENSP00000484318.1:p.Phe270Cys
|
|
NM_001172477.1:c.1187T>G , LRG_788t1:c.1187T>G
|
NP_001165948.1:p.Phe396Cys
|
|
NM_001172478.1:c.815T>G
|
NP_001165949.1:p.Phe272Cys
|
|
NM_015713.4:c.971T>G , LRG_788t2:c.971T>G
|
NP_056528.2:p.Phe324Cys
|
|
NM_001172478.2:c.815T>G
|
NP_001165949.1:p.Phe272Cys
|
|
NM_015713.5:c.971T>G
MANE Select
|
NP_056528.2:p.Phe324Cys
|
|