ENST00000477151.2:n.213C>G
|
|
|
ENST00000643794.1:c.146C>G
|
ENSP00000495765.1:p.Ser49Ter
|
|
ENST00000651669.1:c.25C>G
MANE Select
|
ENSP00000499044.1:p.His9Asp
|
|
ENST00000368567.4:c.25C>G
|
ENSP00000357555.4:p.His9Asp
|
|
ENST00000392558.4:c.25C>G
|
ENSP00000376341.4:p.His9Asp
|
|
ENST00000477151.1:n.180C>G
|
|
|
ENST00000493224.5:n.291C>G
|
|
|
NM_001030.4:c.25C>G
|
NP_001021.1:p.His9Asp
|
|
NM_001030.6:c.25C>G
MANE Select
|
NP_001021.1:p.His9Asp
|
|
NM_001349946.1:c.-72C>G
|
NP_001336875.1:n.-72C>G
|
|
NM_001349947.1:c.-72C>G
|
NP_001336876.1:n.-72C>G
|
|
NM_001349946.2:c.-72C>G
|
NP_001336875.1:n.-72C>G
|
|
NM_001349947.2:c.-72C>G
|
NP_001336876.1:n.-72C>G
|
|