ENST00000426263.10:c.938C>G
MANE Select
|
ENSP00000416293.2:p.Ser313Cys
|
|
ENST00000674545.1:n.256C>G
|
|
|
ENST00000674765.1:c.938C>G
|
ENSP00000501811.1:p.Ser313Cys
|
|
ENST00000675112.1:n.1239C>G
|
|
|
ENST00000676254.1:n.1387C>G
|
|
|
ENST00000426263.7:c.938C>G
|
ENSP00000416293.2:p.Ser313Cys
|
|
ENST00000439722.2:c.817C>G
|
ENSP00000395521.2:n.817C>G
|
|
ENST00000475162.3:c.415+1382C>G
|
|
|
ENST00000630287.2:c.*253C>G
|
ENSP00000486694.1:n.*253C>G
|
|
NM_006516.2:c.938C>G
|
NP_006507.2:p.Ser313Cys
|
|
NM_006516.3:c.938C>G
|
NP_006507.2:p.Ser313Cys
|
|
NM_006516.4:c.938C>G
MANE Select
|
NP_006507.2:p.Ser313Cys
|
|