ENST00000403733.8:c.3167G>T
MANE Select
|
ENSP00000384222.3:p.Arg1056Ile
|
|
ENST00000403733.7:c.3167G>T
|
ENSP00000384222.3:p.Arg1056Ile
|
|
ENST00000427431.5:c.*2559G>T
|
ENSP00000393342.1:n.*2559G>T
|
|
ENST00000438543.5:c.*963G>T
|
ENSP00000413521.1:n.*963G>T
|
|
ENST00000448232.6:c.3239G>T
|
ENSP00000398577.2:p.Arg1080Ile
|
|
ENST00000504005.5:c.2213G>T
|
ENSP00000427569.1:p.Arg738Ile
|
|
ENST00000508747.1:c.551G>T
|
ENSP00000420835.1:p.Arg184Ile
|
|
ENST00000513834.5:c.3020G>T
|
ENSP00000425054.1:p.Arg1007Ile
|
|
NM_024949.5:c.3167G>T
|
NP_079225.5:p.Arg1056Ile
|
|
XM_011532269.1:c.3239G>T
|
XP_011530571.1:p.Arg1080Ile
|
|
XM_011532269.3:c.3239G>T
|
XP_011530571.1:p.Arg1080Ile
|
|
XM_024454225.1:c.2945G>T
|
XP_024309993.1:p.Arg982Ile
|
|
NM_024949.6:c.3167G>T
MANE Select
|
NP_079225.5:p.Arg1056Ile
|
|