ENST00000222572.8:c.932C>G
MANE Select
|
ENSP00000222572.3:p.Ser311Cys
|
|
ENST00000222572.7:c.932C>G
|
ENSP00000222572.3:p.Ser311Cys
|
|
ENST00000433091.6:c.896C>G
|
ENSP00000404622.2:p.Ser299Cys
|
|
ENST00000446142.5:c.*797C>G
|
ENSP00000405211.1:n.*797C>G
|
|
ENST00000455123.5:c.*219C>G
|
ENSP00000414515.1:n.*219C>G
|
|
ENST00000483292.5:c.514C>G
|
|
|
ENST00000633192.1:c.995C>G
|
ENSP00000488378.1:p.Ser332Cys
|
|
ENST00000633531.1:c.932C>G
|
ENSP00000488838.1:p.Ser311Cys
|
|
NM_000305.2:c.932C>G
|
NP_000296.2:p.Ser311Cys
|
|
NM_001018161.1:c.896C>G
|
NP_001018171.1:p.Ser299Cys
|
|
XM_005250453.1:c.728C>G
|
XP_005250510.1:p.Ser243Cys
|
|
XM_005250454.1:c.722C>G
|
XP_005250511.1:p.Ser241Cys
|
|
XM_011516333.1:c.674C>G
|
XP_011514635.1:p.Ser225Cys
|
|
XM_017012357.2:c.722C>G
|
XP_016867846.1:p.Ser241Cys
|
|
XM_017012358.2:c.674C>G
|
XP_016867847.1:p.Ser225Cys
|
|
NM_000305.3:c.932C>G
MANE Select
|
NP_000296.2:p.Ser311Cys
|
|
NM_001018161.2:c.896C>G
|
NP_001018171.1:p.Ser299Cys
|
|