ENST00000403733.8:c.3248T>A
MANE Select
|
ENSP00000384222.3:p.Leu1083His
|
|
ENST00000403733.7:c.3248T>A
|
ENSP00000384222.3:p.Leu1083His
|
|
ENST00000427431.5:c.*2640T>A
|
ENSP00000393342.1:n.*2640T>A
|
|
ENST00000438543.5:c.*1044T>A
|
ENSP00000413521.1:n.*1044T>A
|
|
ENST00000448232.6:c.3320T>A
|
ENSP00000398577.2:p.Leu1107His
|
|
ENST00000504005.5:c.2294T>A
|
ENSP00000427569.1:p.Leu765His
|
|
ENST00000508747.1:c.632T>A
|
ENSP00000420835.1:p.Leu211His
|
|
ENST00000513834.5:c.3101T>A
|
ENSP00000425054.1:p.Leu1034His
|
|
NM_024949.5:c.3248T>A
|
NP_079225.5:p.Leu1083His
|
|
XM_011532269.1:c.3320T>A
|
XP_011530571.1:p.Leu1107His
|
|
XM_011532269.3:c.3320T>A
|
XP_011530571.1:p.Leu1107His
|
|
XM_024454225.1:c.3026T>A
|
XP_024309993.1:p.Leu1009His
|
|
NM_024949.6:c.3248T>A
MANE Select
|
NP_079225.5:p.Leu1083His
|
|