ENST00000403733.8:c.3350G>T
MANE Select
|
ENSP00000384222.3:p.Arg1117Met
|
|
ENST00000403733.7:c.3350G>T
|
ENSP00000384222.3:p.Arg1117Met
|
|
ENST00000427431.5:c.*2742G>T
|
ENSP00000393342.1:n.*2742G>T
|
|
ENST00000438543.5:c.*1146G>T
|
ENSP00000413521.1:n.*1146G>T
|
|
ENST00000448232.6:c.3422G>T
|
ENSP00000398577.2:p.Arg1141Met
|
|
ENST00000504005.5:c.2396G>T
|
ENSP00000427569.1:p.Arg799Met
|
|
ENST00000508747.1:c.734G>T
|
ENSP00000420835.1:p.Arg245Met
|
|
ENST00000513834.5:c.3203G>T
|
ENSP00000425054.1:p.Arg1068Met
|
|
NM_024949.5:c.3350G>T
|
NP_079225.5:p.Arg1117Met
|
|
XM_011532269.1:c.3422G>T
|
XP_011530571.1:p.Arg1141Met
|
|
XM_011532269.3:c.3422G>T
|
XP_011530571.1:p.Arg1141Met
|
|
XM_024454225.1:c.3128G>T
|
XP_024309993.1:p.Arg1043Met
|
|
NM_024949.6:c.3350G>T
MANE Select
|
NP_079225.5:p.Arg1117Met
|
|