ENST00000480188.2:n.1202C>G
|
|
|
ENST00000696279.1:c.4488C>G
|
|
|
ENST00000696280.1:n.4257C>G
|
|
|
ENST00000696281.1:c.4186C>G
|
ENSP00000512521.1:p.His1396Asp
|
|
ENST00000697921.1:n.3046C>G
|
|
|
ENST00000697922.1:c.*4158C>G
|
ENSP00000513478.1:n.*4158C>G
|
|
ENST00000697923.1:n.4613C>G
|
|
|
ENST00000223642.3:c.4168C>G
MANE Select
|
ENSP00000223642.1:p.His1390Asp
|
|
ENST00000223642.2:c.4168C>G
|
ENSP00000223642.1:p.His1390Asp
|
|
NM_001735.2:c.4168C>G , LRG_28t1:c.4168C>G
|
NP_001726.2:p.His1390Asp
|
|
XM_011518980.1:c.4183C>G
|
XP_011517282.1:p.His1395Asp
|
|
NM_001317163.1:c.4186C>G
|
NP_001304092.1:p.His1396Asp
|
|
NM_001317163.2:c.4186C>G
|
NP_001304092.1:p.His1396Asp
|
|
NM_001735.3:c.4168C>G
MANE Select
|
NP_001726.2:p.His1390Asp
|
|