ENST00000378482.7:c.460C>T
MANE Select
|
ENSP00000367743.2:p.Gln154Ter
|
|
ENST00000286824.6:c.511C>T
|
ENSP00000286824.6:p.Gln171Ter
|
|
ENST00000378482.6:c.460C>T
|
ENSP00000367743.2:p.Gln154Ter
|
|
ENST00000419600.3:n.404C>T
|
|
|
ENST00000465127.1:c.550C>T
|
ENSP00000417050.1:p.Gln184Ter
|
|
ENST00000471410.5:c.*486C>T
|
ENSP00000419290.1:n.*486C>T
|
|
ENST00000475216.5:c.*453C>T
|
ENSP00000418586.1:n.*453C>T
|
|
ENST00000488893.5:n.643C>T
|
|
|
NM_004615.3:c.460C>T
|
NP_004606.2:p.Gln154Ter
|
|
NM_004615.4:c.460C>T
MANE Select
|
NP_004606.2:p.Gln154Ter
|
|