ENST00000392676.8:c.4275T>G
MANE Select
|
ENSP00000376443.2:p.His1425Gln
|
|
ENST00000392676.7:c.4275T>G
|
ENSP00000376443.2:p.His1425Gln
|
|
ENST00000586811.1:c.1173T>G
|
ENSP00000465351.1:p.His391Gln
|
|
ENST00000586995.5:c.3337T>G
|
ENSP00000467251.1:n.3337T>G
|
|
ENST00000588877.5:c.4275T>G
|
ENSP00000467882.1:p.His1425Gln
|
|
ENST00000591234.5:c.2217T>G
|
ENSP00000465766.1:n.2217T>G
|
|
NM_018672.4:c.4275T>G
|
NP_061142.2:p.His1425Gln
|
|
NM_172232.3:c.4275T>G
|
NP_758424.1:p.His1425Gln
|
|
NM_172232.4:c.4275T>G
MANE Select
|
NP_758424.1:p.His1425Gln
|
|
NM_018672.5:c.4275T>G
|
NP_061142.2:p.His1425Gln
|
|