ENST00000682276.1:n.1204T>G
|
|
|
ENST00000682892.1:c.1306T>G
|
ENSP00000507214.1:p.Ser436Ala
|
|
ENST00000682952.1:n.1398T>G
|
|
|
ENST00000684455.1:c.972T>G
|
|
|
ENST00000684642.1:c.1156T>G
|
ENSP00000507355.1:p.Ser386Ala
|
|
ENST00000303236.9:c.1759T>G
MANE Select
|
ENSP00000307235.3:p.Ser587Ala
|
|
ENST00000652099.1:c.1953T>G
|
|
|
ENST00000652736.1:n.1635T>G
|
|
|
ENST00000303236.7:c.1759T>G
|
ENSP00000307235.3:p.Ser587Ala
|
|
ENST00000415570.1:c.1396T>G
|
ENSP00000412076.1:p.Ser466Ala
|
|
ENST00000419748.5:c.1306T>G
|
ENSP00000408325.1:p.Ser436Ala
|
|
NM_001313915.1:c.1306T>G
|
NP_001300844.1:p.Ser436Ala
|
|
NM_004836.5:c.1759T>G
|
NP_004827.4:p.Ser587Ala
|
|
NM_004836.6:c.1759T>G
|
NP_004827.4:p.Ser587Ala
|
|
XM_005264649.3:c.1075T>G
|
XP_005264706.1:p.Ser359Ala
|
|
XR_939749.1:n.1968T>G
|
|
|
XM_017005376.2:c.1075T>G
|
XP_016860865.1:p.Ser359Ala
|
|
NM_004836.7:c.1759T>G
MANE Select
|
NP_004827.4:p.Ser587Ala
|
|
NM_001313915.2:c.1306T>G
|
NP_001300844.1:p.Ser436Ala
|
|