ENST00000261304.7:c.711G>T
MANE Select
|
ENSP00000261304.2:p.Met237Ile
|
|
ENST00000261304.6:c.711G>T
|
ENSP00000261304.2:p.Met237Ile
|
|
ENST00000393568.8:c.642G>T
|
ENSP00000377198.4:p.Met214Ile
|
|
ENST00000393569.6:c.633G>T
|
ENSP00000377199.2:p.Met211Ile
|
|
ENST00000474294.6:n.701G>T
|
|
|
ENST00000477716.3:n.466G>T
|
|
|
ENST00000544807.6:c.543G>T
|
ENSP00000437513.2:p.Met181Ile
|
|
ENST00000554916.5:n.590G>T
|
|
|
ENST00000555000.5:c.78G>T
|
ENSP00000450472.1:p.Met26Ile
|
|
ENST00000557316.5:c.*109G>T
|
ENSP00000452314.1:n.*109G>T
|
|
ENST00000622264.4:c.701G>T
|
|
|
NM_000153.3:c.711G>T
|
NP_000144.2:p.Met237Ile
|
|
NM_001201401.1:c.642G>T
|
NP_001188330.1:p.Met214Ile
|
|
NM_001201402.1:c.633G>T
|
NP_001188331.1:p.Met211Ile
|
|
XM_011536618.1:c.543G>T
|
XP_011534920.1:p.Met181Ile
|
|
XM_011536618.2:c.543G>T
|
XP_011534920.1:p.Met181Ile
|
|
NM_000153.4:c.711G>T
MANE Select
|
NP_000144.2:p.Met237Ile
|
|
NM_001201401.2:c.642G>T
|
NP_001188330.1:p.Met214Ile
|
|
NM_001201402.2:c.633G>T
|
NP_001188331.1:p.Met211Ile
|
|