ENST00000403733.8:c.3340G>A
MANE Select
|
ENSP00000384222.3:p.Glu1114Lys
|
|
ENST00000403733.7:c.3340G>A
|
ENSP00000384222.3:p.Glu1114Lys
|
|
ENST00000427431.5:c.*2732G>A
|
ENSP00000393342.1:n.*2732G>A
|
|
ENST00000438543.5:c.*1136G>A
|
ENSP00000413521.1:n.*1136G>A
|
|
ENST00000448232.6:c.3412G>A
|
ENSP00000398577.2:p.Glu1138Lys
|
|
ENST00000504005.5:c.2386G>A
|
ENSP00000427569.1:p.Glu796Lys
|
|
ENST00000508747.1:c.724G>A
|
ENSP00000420835.1:p.Glu242Lys
|
|
ENST00000513834.5:c.3193G>A
|
ENSP00000425054.1:p.Glu1065Lys
|
|
NM_024949.5:c.3340G>A
|
NP_079225.5:p.Glu1114Lys
|
|
XM_011532269.1:c.3412G>A
|
XP_011530571.1:p.Glu1138Lys
|
|
XM_011532269.3:c.3412G>A
|
XP_011530571.1:p.Glu1138Lys
|
|
XM_024454225.1:c.3118G>A
|
XP_024309993.1:p.Glu1040Lys
|
|
NM_024949.6:c.3340G>A
MANE Select
|
NP_079225.5:p.Glu1114Lys
|
|