ENST00000378482.7:c.544A>T
MANE Select
|
ENSP00000367743.2:p.Asn182Tyr
|
|
ENST00000286824.6:c.595A>T
|
ENSP00000286824.6:p.Asn199Tyr
|
|
ENST00000378482.6:c.544A>T
|
ENSP00000367743.2:p.Asn182Tyr
|
|
ENST00000419600.3:n.488A>T
|
|
|
ENST00000465127.1:c.634A>T
|
ENSP00000417050.1:p.Asn212Tyr
|
|
ENST00000471410.5:c.*570A>T
|
ENSP00000419290.1:n.*570A>T
|
|
ENST00000475216.5:c.*537A>T
|
ENSP00000418586.1:n.*537A>T
|
|
ENST00000488893.5:n.727A>T
|
|
|
NM_004615.3:c.544A>T
|
NP_004606.2:p.Asn182Tyr
|
|
NM_004615.4:c.544A>T
MANE Select
|
NP_004606.2:p.Asn182Tyr
|
|