ENST00000374552.9:c.941T>G
MANE Select
|
ENSP00000363680.4:p.Phe314Cys
|
|
ENST00000374552.8:c.941T>G
|
ENSP00000363680.4:p.Phe314Cys
|
|
ENST00000374553.6:c.935T>G
|
ENSP00000363681.2:p.Phe312Cys
|
|
ENST00000524573.5:c.926T>G
|
ENSP00000432585.1:p.Phe309Cys
|
|
ENST00000616899.1:c.545T>G
|
ENSP00000481963.1:p.Phe182Cys
|
|
NM_001005609.1:c.935T>G
|
NP_001005609.1:p.Phe312Cys
|
|
NM_001005612.2:c.926T>G
|
NP_001005612.2:p.Phe309Cys
|
|
NM_001399.4:c.941T>G
|
NP_001390.1:p.Phe314Cys
|
|
XM_006724630.2:c.932T>G
|
XP_006724693.1:p.Phe311Cys
|
|
XM_017029336.1:c.899T>G
|
XP_016884825.1:p.Phe300Cys
|
|
NM_001399.5:c.941T>G
MANE Select
|
NP_001390.1:p.Phe314Cys
|
|
NM_001005609.2:c.935T>G
|
NP_001005609.1:p.Phe312Cys
|
|
NM_001005612.3:c.926T>G
|
NP_001005612.2:p.Phe309Cys
|
|