ENST00000477151.2:n.102C>G
|
|
|
ENST00000643794.1:c.115C>G
|
ENSP00000495765.1:p.Arg39Gly
|
|
ENST00000651669.1:c.7-93C>G
MANE Select
|
ENSP00000499044.1:n.7-93C>G
|
|
ENST00000368567.4:c.7-93C>G
|
ENSP00000357555.4:n.7-93C>G
|
|
ENST00000392558.4:c.7-93C>G
|
ENSP00000376341.4:n.7-93C>G
|
|
ENST00000477151.1:n.149C>G
|
|
|
ENST00000493224.5:n.260C>G
|
|
|
NM_001030.4:c.7-93C>G
|
NP_001021.1:n.7-93C>G
|
|
NM_001030.6:c.7-93C>G
MANE Select
|
NP_001021.1:n.7-93C>G
|
|
NM_001349946.1:c.-103C>G
|
NP_001336875.1:n.-103C>G
|
|
NM_001349947.1:c.-103C>G
|
NP_001336876.1:n.-103C>G
|
|
NM_001349946.2:c.-103C>G
|
NP_001336875.1:n.-103C>G
|
|
NM_001349947.2:c.-103C>G
|
NP_001336876.1:n.-103C>G
|
|