ENST00000261304.7:c.710T>G
MANE Select
|
ENSP00000261304.2:p.Met237Arg
|
|
ENST00000261304.6:c.710T>G
|
ENSP00000261304.2:p.Met237Arg
|
|
ENST00000393568.8:c.641T>G
|
ENSP00000377198.4:p.Met214Arg
|
|
ENST00000393569.6:c.632T>G
|
ENSP00000377199.2:p.Met211Arg
|
|
ENST00000474294.6:n.700T>G
|
|
|
ENST00000477716.3:n.465T>G
|
|
|
ENST00000544807.6:c.542T>G
|
ENSP00000437513.2:p.Met181Arg
|
|
ENST00000554916.5:n.589T>G
|
|
|
ENST00000555000.5:c.77T>G
|
ENSP00000450472.1:p.Met26Arg
|
|
ENST00000557316.5:c.*108T>G
|
ENSP00000452314.1:n.*108T>G
|
|
ENST00000622264.4:c.700T>G
|
|
|
NM_000153.3:c.710T>G
|
NP_000144.2:p.Met237Arg
|
|
NM_001201401.1:c.641T>G
|
NP_001188330.1:p.Met214Arg
|
|
NM_001201402.1:c.632T>G
|
NP_001188331.1:p.Met211Arg
|
|
XM_011536618.1:c.542T>G
|
XP_011534920.1:p.Met181Arg
|
|
XM_011536618.2:c.542T>G
|
XP_011534920.1:p.Met181Arg
|
|
NM_000153.4:c.710T>G
MANE Select
|
NP_000144.2:p.Met237Arg
|
|
NM_001201401.2:c.641T>G
|
NP_001188330.1:p.Met214Arg
|
|
NM_001201402.2:c.632T>G
|
NP_001188331.1:p.Met211Arg
|
|