ENST00000378482.7:c.442-183T>G
MANE Select
|
ENSP00000367743.2:n.442-183T>G
|
|
ENST00000286824.6:c.493-183T>G
|
ENSP00000286824.6:n.493-183T>G
|
|
ENST00000378482.6:c.442-183T>G
|
ENSP00000367743.2:n.442-183T>G
|
|
ENST00000419600.3:n.386-183T>G
|
|
|
ENST00000465127.1:c.532-183T>G
|
ENSP00000417050.1:n.532-183T>G
|
|
ENST00000471410.5:c.*468-183T>G
|
ENSP00000419290.1:n.*468-183T>G
|
|
ENST00000475216.5:c.*435-183T>G
|
ENSP00000418586.1:n.*435-183T>G
|
|
ENST00000488893.5:n.625-183T>G
|
|
|
NM_004615.3:c.442-183T>G
|
NP_004606.2:n.442-183T>G
|
|
NM_004615.4:c.442-183T>G
MANE Select
|
NP_004606.2:n.442-183T>G
|
|