ENST00000369458.8:c.841C=
MANE Select
|
ENSP00000358470.3:p.Leu281=
|
|
ENST00000328189.7:c.493C=
|
ENSP00000328168.3:p.Leu165=
|
|
ENST00000359008.8:c.850C=
|
ENSP00000351899.4:p.Leu284=
|
|
ENST00000369458.7:c.841C=
|
ENSP00000358470.3:p.Leu281=
|
|
ENST00000539893.5:c.556C=
|
ENSP00000444724.1:p.Leu186=
|
|
NM_001253849.1:c.556C=
|
NP_001240778.1:p.Leu186=
|
|
NM_001253850.1:c.493C=
|
NP_001240779.1:p.Leu165=
|
|
NM_024626.3:c.841C=
|
NP_078902.2:p.Leu281=
|
|
NR_045603.1:n.1036C=
|
|
|
NR_045604.1:n.740C=
|
|
|
XM_011542143.1:c.892C=
|
XP_011540445.1:p.Leu298=
|
|
XM_011542144.1:c.895C=
|
XP_011540446.1:p.Leu299=
|
|
XM_011542145.1:c.856C=
|
XP_011540447.1:p.Leu286=
|
|
XM_011542143.2:c.991C=
|
XP_011540445.2:p.Leu331=
|
|
XM_017002335.2:c.856C=
|
XP_016857824.1:p.Leu286=
|
|
NM_024626.4:c.841C=
MANE Select
|
NP_078902.2:p.Leu281=
|
|
NR_045603.2:n.1003C=
|
|
|
NR_045604.2:n.707C=
|
|
|
NM_001253849.2:c.556C=
|
NP_001240778.1:p.Leu186=
|
|
NM_001253850.2:c.493C=
|
NP_001240779.1:p.Leu165=
|
|