ENST00000237014.8:c.427_433delinsACCAATC
MANE Select
|
ENSP00000237014.4:p.Thr143=
|
|
ENST00000610404.5:c.331_337delinsACCAATC
|
ENSP00000477599.2:p.Thr111=
|
|
ENST00000649620.1:c.427_433delinsACCAATC
|
ENSP00000497927.1:p.Thr143=
|
|
ENST00000237014.7:c.427_433delinsACCAATC
|
ENSP00000237014.3:p.Thr143=
|
|
ENST00000610404.4:c.541_547delinsACCAATC
|
ENSP00000477599.1:p.Thr181=
|
|
ENST00000613781.1:c.403_409delinsACCAATC
|
ENSP00000479174.1:p.Thr135=
|
|
NM_000371.3:c.427_433delinsACCAATC , LRG_416t1:c.427_433delinsACCAATC
|
NP_000362.1:p.Thr143=
|
|
NM_000371.4:c.427_433delinsACCAATC
MANE Select
|
NP_000362.1:p.Thr143=
|
|