ENST00000344408.10:c.1735T>G
MANE Select
|
ENSP00000342144.5:p.Phe579Val
|
|
ENST00000310917.6:c.1495T>G
|
ENSP00000311683.2:p.Phe499Val
|
|
ENST00000344408.9:c.1735T>G
|
ENSP00000342144.5:p.Phe579Val
|
|
ENST00000475313.5:c.1495T>G
|
ENSP00000431981.1:p.Phe499Val
|
|
ENST00000509670.1:c.*128T>G
|
ENSP00000423876.1:n.*128T>G
|
|
NM_001166136.1:c.1495T>G
|
NP_001159608.1:p.Phe499Val
|
|
NM_147127.4:c.1735T>G
|
NP_667338.3:p.Phe579Val
|
|
XM_011513392.1:c.1744T>G
|
XP_011511694.1:p.Phe582Val
|
|
XM_011513393.1:c.1744T>G
|
XP_011511695.1:p.Phe582Val
|
|
XM_011513394.1:c.1504T>G
|
XP_011511696.1:p.Phe502Val
|
|
XM_017007736.1:c.1495T>G
|
XP_016863225.1:p.Phe499Val
|
|
XM_017007737.1:c.1495T>G
|
XP_016863226.1:p.Phe499Val
|
|
XM_017007738.1:c.1735T>G
|
XP_016863227.1:p.Phe579Val
|
|
XM_017007739.1:c.55T>G
|
XP_016863228.1:p.Phe19Val
|
|
XM_024453893.1:c.55T>G
|
XP_024309661.1:p.Phe19Val
|
|
XR_001741141.1:n.1800T>G
|
|
|
NM_147127.5:c.1735T>G
MANE Select
|
NP_667338.3:p.Phe579Val
|
|
NM_001166136.2:c.1495T>G
|
NP_001159608.1:p.Phe499Val
|
|