ENST00000378482.7:c.546T>G
MANE Select
|
ENSP00000367743.2:p.Asn182Lys
|
|
ENST00000286824.6:c.597T>G
|
ENSP00000286824.6:p.Asn199Lys
|
|
ENST00000378482.6:c.546T>G
|
ENSP00000367743.2:p.Asn182Lys
|
|
ENST00000419600.3:n.490T>G
|
|
|
ENST00000465127.1:c.636T>G
|
ENSP00000417050.1:p.Asn212Lys
|
|
ENST00000471410.5:c.*572T>G
|
ENSP00000419290.1:n.*572T>G
|
|
ENST00000475216.5:c.*539T>G
|
ENSP00000418586.1:n.*539T>G
|
|
ENST00000488893.5:n.729T>G
|
|
|
NM_004615.3:c.546T>G
|
NP_004606.2:p.Asn182Lys
|
|
NM_004615.4:c.546T>G
MANE Select
|
NP_004606.2:p.Asn182Lys
|
|