ENST00000274576.9:c.785T>G
MANE Select
|
ENSP00000274576.5:p.Ile262Ser
|
|
ENST00000274576.8:c.785T>G
|
ENSP00000274576.4:p.Ile262Ser
|
|
ENST00000455880.2:c.785T>G
|
ENSP00000411593.2:p.Ile262Ser
|
|
ENST00000462581.6:c.*543T>G
|
ENSP00000430595.1:n.*543T>G
|
|
ENST00000471351.2:n.1068T>G
|
|
|
NM_000171.3:c.785T>G
|
NP_000162.2:p.Ile262Ser
|
|
NM_001146040.1:c.785T>G
|
NP_001139512.1:p.Ile262Ser
|
|
NM_001292000.1:c.536T>G
|
NP_001278929.1:p.Ile179Ser
|
|
XM_005268412.2:c.785T>G
|
XP_005268469.1:p.Ile262Ser
|
|
NM_000171.4:c.785T>G
MANE Select
|
NP_000162.2:p.Ile262Ser
|
|
NM_001146040.2:c.785T>G
|
NP_001139512.1:p.Ile262Ser
|
|
NM_001292000.2:c.536T>G
|
NP_001278929.1:p.Ile179Ser
|
|