ENST00000403733.8:c.3256G>A
MANE Select
|
ENSP00000384222.3:p.Glu1086Lys
|
|
ENST00000403733.7:c.3256G>A
|
ENSP00000384222.3:p.Glu1086Lys
|
|
ENST00000427431.5:c.*2648G>A
|
ENSP00000393342.1:n.*2648G>A
|
|
ENST00000438543.5:c.*1052G>A
|
ENSP00000413521.1:n.*1052G>A
|
|
ENST00000448232.6:c.3328G>A
|
ENSP00000398577.2:p.Glu1110Lys
|
|
ENST00000504005.5:c.2302G>A
|
ENSP00000427569.1:p.Glu768Lys
|
|
ENST00000508747.1:c.640G>A
|
ENSP00000420835.1:p.Glu214Lys
|
|
ENST00000513834.5:c.3109G>A
|
ENSP00000425054.1:p.Glu1037Lys
|
|
NM_024949.5:c.3256G>A
|
NP_079225.5:p.Glu1086Lys
|
|
XM_011532269.1:c.3328G>A
|
XP_011530571.1:p.Glu1110Lys
|
|
XM_011532269.3:c.3328G>A
|
XP_011530571.1:p.Glu1110Lys
|
|
XM_024454225.1:c.3034G>A
|
XP_024309993.1:p.Glu1012Lys
|
|
NM_024949.6:c.3256G>A
MANE Select
|
NP_079225.5:p.Glu1086Lys
|
|