ENST00000369458.8:c.797T>C
MANE Select
|
ENSP00000358470.3:p.Phe266Ser
|
|
ENST00000328189.7:c.449T>C
|
ENSP00000328168.3:p.Phe150Ser
|
|
ENST00000359008.8:c.806T>C
|
ENSP00000351899.4:p.Phe269Ser
|
|
ENST00000369458.7:c.797T>C
|
ENSP00000358470.3:p.Phe266Ser
|
|
ENST00000539893.5:c.512T>C
|
ENSP00000444724.1:p.Phe171Ser
|
|
NM_001253849.1:c.512T>C
|
NP_001240778.1:p.Phe171Ser
|
|
NM_001253850.1:c.449T>C
|
NP_001240779.1:p.Phe150Ser
|
|
NM_024626.3:c.797T>C
|
NP_078902.2:p.Phe266Ser
|
|
NR_045603.1:n.992T>C
|
|
|
NR_045604.1:n.696T>C
|
|
|
XM_011542143.1:c.848T>C
|
XP_011540445.1:p.Phe283Ser
|
|
XM_011542144.1:c.851T>C
|
XP_011540446.1:p.Phe284Ser
|
|
XM_011542145.1:c.812T>C
|
XP_011540447.1:p.Phe271Ser
|
|
XM_011542143.2:c.947T>C
|
XP_011540445.2:p.Phe316Ser
|
|
XM_017002335.2:c.812T>C
|
XP_016857824.1:p.Phe271Ser
|
|
NM_024626.4:c.797T>C
MANE Select
|
NP_078902.2:p.Phe266Ser
|
|
NR_045603.2:n.959T>C
|
|
|
NR_045604.2:n.663T>C
|
|
|
NM_001253849.2:c.512T>C
|
NP_001240778.1:p.Phe171Ser
|
|
NM_001253850.2:c.449T>C
|
NP_001240779.1:p.Phe150Ser
|
|