ENST00000336180.7:c.1668C>A
MANE Select
|
ENSP00000336740.2:p.Thr556=
|
|
ENST00000336180.6:c.1668C>A
|
ENSP00000336740.2:p.Thr556=
|
|
ENST00000418310.5:c.1758C>A
|
ENSP00000409717.1:p.Thr586=
|
|
ENST00000435201.5:c.1607C>A
|
ENSP00000414606.1:n.1607C>A
|
|
ENST00000476792.1:n.692C>A
|
|
|
ENST00000538333.3:c.1566C>A
|
ENSP00000444452.1:p.Thr522=
|
|
NM_001204426.1:c.1566C>A
|
NP_001191355.1:p.Thr522=
|
|
NM_002314.3:c.1668C>A
|
NP_002305.1:p.Thr556=
|
|
NM_002314.4:c.1668C>A
MANE Select
|
NP_002305.1:p.Thr556=
|
|
NM_001204426.2:c.1566C>A
|
NP_001191355.1:p.Thr522=
|
|