ENST00000426263.10:c.803A>G
MANE Select
|
ENSP00000416293.2:p.Tyr268Cys
|
|
ENST00000669445.1:c.133A>G
|
|
|
ENST00000674765.1:c.803A>G
|
ENSP00000501811.1:p.Tyr268Cys
|
|
ENST00000675112.1:n.826A>G
|
|
|
ENST00000676254.1:n.1252A>G
|
|
|
ENST00000426263.7:c.803A>G
|
ENSP00000416293.2:p.Tyr268Cys
|
|
ENST00000439722.2:c.682A>G
|
ENSP00000395521.2:n.682A>G
|
|
ENST00000475162.3:c.415+969A>G
|
|
|
ENST00000630287.2:c.*118A>G
|
ENSP00000486694.1:n.*118A>G
|
|
NM_006516.2:c.803A>G
|
NP_006507.2:p.Tyr268Cys
|
|
NM_006516.3:c.803A>G
|
NP_006507.2:p.Tyr268Cys
|
|
NM_006516.4:c.803A>G
MANE Select
|
NP_006507.2:p.Tyr268Cys
|
|