ENST00000336180.7:c.339G>A
MANE Select
|
ENSP00000336740.2:p.Thr113=
|
|
ENST00000336180.6:c.339G>A
|
ENSP00000336740.2:p.Thr113=
|
|
ENST00000418310.5:c.429G>A
|
ENSP00000409717.1:p.Thr143=
|
|
ENST00000435201.5:c.339G>A
|
ENSP00000414606.1:p.Thr113=
|
|
ENST00000483414.1:n.25G>A
|
|
|
ENST00000486361.5:n.507G>A
|
|
|
ENST00000491052.5:n.287G>A
|
|
|
ENST00000538333.3:c.237G>A
|
ENSP00000444452.1:p.Thr79=
|
|
NM_001204426.1:c.237G>A
|
NP_001191355.1:p.Thr79=
|
|
NM_002314.3:c.339G>A
|
NP_002305.1:p.Thr113=
|
|
NM_002314.4:c.339G>A
MANE Select
|
NP_002305.1:p.Thr113=
|
|
NM_001204426.2:c.237G>A
|
NP_001191355.1:p.Thr79=
|
|