ENST00000378482.7:c.548C>A
MANE Select
|
ENSP00000367743.2:p.Pro183His
|
|
ENST00000286824.6:c.599C>A
|
ENSP00000286824.6:p.Pro200His
|
|
ENST00000378482.6:c.548C>A
|
ENSP00000367743.2:p.Pro183His
|
|
ENST00000419600.3:n.492C>A
|
|
|
ENST00000465127.1:c.638C>A
|
ENSP00000417050.1:p.Pro213His
|
|
ENST00000471410.5:c.*574C>A
|
ENSP00000419290.1:n.*574C>A
|
|
ENST00000475216.5:c.*541C>A
|
ENSP00000418586.1:n.*541C>A
|
|
ENST00000488893.5:n.731C>A
|
|
|
NM_004615.3:c.548C>A
|
NP_004606.2:p.Pro183His
|
|
NM_004615.4:c.548C>A
MANE Select
|
NP_004606.2:p.Pro183His
|
|