ENST00000261304.7:c.636G>A
MANE Select
|
ENSP00000261304.2:p.Met212Ile
|
|
ENST00000261304.6:c.636G>A
|
ENSP00000261304.2:p.Met212Ile
|
|
ENST00000393568.8:c.567G>A
|
ENSP00000377198.4:p.Met189Ile
|
|
ENST00000393569.6:c.558G>A
|
ENSP00000377199.2:p.Met186Ile
|
|
ENST00000474294.6:n.626G>A
|
|
|
ENST00000477716.3:n.391G>A
|
|
|
ENST00000544807.6:c.468G>A
|
ENSP00000437513.2:p.Met156Ile
|
|
ENST00000554916.5:n.515G>A
|
|
|
ENST00000555000.5:c.3G>A
|
ENSP00000450472.1:p.Met1Ile
|
|
ENST00000557316.5:c.*34G>A
|
ENSP00000452314.1:n.*34G>A
|
|
ENST00000622264.4:c.626G>A
|
|
|
NM_000153.3:c.636G>A
|
NP_000144.2:p.Met212Ile
|
|
NM_001201401.1:c.567G>A
|
NP_001188330.1:p.Met189Ile
|
|
NM_001201402.1:c.558G>A
|
NP_001188331.1:p.Met186Ile
|
|
XM_011536618.1:c.468G>A
|
XP_011534920.1:p.Met156Ile
|
|
XM_011536618.2:c.468G>A
|
XP_011534920.1:p.Met156Ile
|
|
NM_000153.4:c.636G>A
MANE Select
|
NP_000144.2:p.Met212Ile
|
|
NM_001201401.2:c.567G>A
|
NP_001188330.1:p.Met189Ile
|
|
NM_001201402.2:c.558G>A
|
NP_001188331.1:p.Met186Ile
|
|