ENST00000367651.4:c.664T>G
MANE Select
|
ENSP00000356623.2:p.Phe222Val
|
|
ENST00000367651.3:c.664T>G
|
ENSP00000356623.2:p.Phe222Val
|
|
ENST00000536159.2:c.664T>G
|
ENSP00000442831.1:p.Phe222Val
|
|
ENST00000537332.2:c.679T>G
|
ENSP00000444198.2:p.Phe227Val
|
|
ENST00000618718.1:c.493T>G
|
ENSP00000479918.1:p.Phe165Val
|
|
NM_001168388.2:c.664T>G
|
NP_001161860.1:p.Phe222Val
|
|
NM_001168389.2:c.679T>G
|
NP_001161861.2:p.Phe227Val
|
|
NM_006079.4:c.664T>G
|
NP_006070.2:p.Phe222Val
|
|
NM_006079.5:c.664T>G
MANE Select
|
NP_006070.2:p.Phe222Val
|
|
NM_001168388.3:c.664T>G
|
NP_001161860.1:p.Phe222Val
|
|
NM_001168389.3:c.679T>G
|
NP_001161861.2:p.Phe227Val
|
|