ENST00000374552.9:c.941T>A
MANE Select
|
ENSP00000363680.4:p.Phe314Tyr
|
|
ENST00000374552.8:c.941T>A
|
ENSP00000363680.4:p.Phe314Tyr
|
|
ENST00000374553.6:c.935T>A
|
ENSP00000363681.2:p.Phe312Tyr
|
|
ENST00000524573.5:c.926T>A
|
ENSP00000432585.1:p.Phe309Tyr
|
|
ENST00000616899.1:c.545T>A
|
ENSP00000481963.1:p.Phe182Tyr
|
|
NM_001005609.1:c.935T>A
|
NP_001005609.1:p.Phe312Tyr
|
|
NM_001005612.2:c.926T>A
|
NP_001005612.2:p.Phe309Tyr
|
|
NM_001399.4:c.941T>A
|
NP_001390.1:p.Phe314Tyr
|
|
XM_006724630.2:c.932T>A
|
XP_006724693.1:p.Phe311Tyr
|
|
XM_017029336.1:c.899T>A
|
XP_016884825.1:p.Phe300Tyr
|
|
NM_001399.5:c.941T>A
MANE Select
|
NP_001390.1:p.Phe314Tyr
|
|
NM_001005609.2:c.935T>A
|
NP_001005609.1:p.Phe312Tyr
|
|
NM_001005612.3:c.926T>A
|
NP_001005612.2:p.Phe309Tyr
|
|