ENST00000369458.8:c.793T>A
MANE Select
|
ENSP00000358470.3:p.Phe265Ile
|
|
ENST00000328189.7:c.445T>A
|
ENSP00000328168.3:p.Phe149Ile
|
|
ENST00000359008.8:c.802T>A
|
ENSP00000351899.4:p.Phe268Ile
|
|
ENST00000369458.7:c.793T>A
|
ENSP00000358470.3:p.Phe265Ile
|
|
ENST00000539893.5:c.508T>A
|
ENSP00000444724.1:p.Phe170Ile
|
|
NM_001253849.1:c.508T>A
|
NP_001240778.1:p.Phe170Ile
|
|
NM_001253850.1:c.445T>A
|
NP_001240779.1:p.Phe149Ile
|
|
NM_024626.3:c.793T>A
|
NP_078902.2:p.Phe265Ile
|
|
NR_045603.1:n.988T>A
|
|
|
NR_045604.1:n.692T>A
|
|
|
XM_011542143.1:c.844T>A
|
XP_011540445.1:p.Phe282Ile
|
|
XM_011542144.1:c.847T>A
|
XP_011540446.1:p.Phe283Ile
|
|
XM_011542145.1:c.808T>A
|
XP_011540447.1:p.Phe270Ile
|
|
XM_011542143.2:c.943T>A
|
XP_011540445.2:p.Phe315Ile
|
|
XM_017002335.2:c.808T>A
|
XP_016857824.1:p.Phe270Ile
|
|
NM_024626.4:c.793T>A
MANE Select
|
NP_078902.2:p.Phe265Ile
|
|
NR_045603.2:n.955T>A
|
|
|
NR_045604.2:n.659T>A
|
|
|
NM_001253849.2:c.508T>A
|
NP_001240778.1:p.Phe170Ile
|
|
NM_001253850.2:c.445T>A
|
NP_001240779.1:p.Phe149Ile
|
|