ENST00000403733.8:c.3166A>T
MANE Select
|
ENSP00000384222.3:p.Arg1056Ter
|
|
ENST00000403733.7:c.3166A>T
|
ENSP00000384222.3:p.Arg1056Ter
|
|
ENST00000427431.5:c.*2558A>T
|
ENSP00000393342.1:n.*2558A>T
|
|
ENST00000438543.5:c.*962A>T
|
ENSP00000413521.1:n.*962A>T
|
|
ENST00000448232.6:c.3238A>T
|
ENSP00000398577.2:p.Arg1080Ter
|
|
ENST00000504005.5:c.2212A>T
|
ENSP00000427569.1:p.Arg738Ter
|
|
ENST00000508747.1:c.550A>T
|
ENSP00000420835.1:p.Arg184Ter
|
|
ENST00000513834.5:c.3019A>T
|
ENSP00000425054.1:p.Arg1007Ter
|
|
NM_024949.5:c.3166A>T
|
NP_079225.5:p.Arg1056Ter
|
|
XM_011532269.1:c.3238A>T
|
XP_011530571.1:p.Arg1080Ter
|
|
XM_011532269.3:c.3238A>T
|
XP_011530571.1:p.Arg1080Ter
|
|
XM_024454225.1:c.2944A>T
|
XP_024309993.1:p.Arg982Ter
|
|
NM_024949.6:c.3166A>T
MANE Select
|
NP_079225.5:p.Arg1056Ter
|
|