ENST00000378482.7:c.499G>C
MANE Select
|
ENSP00000367743.2:p.Glu167Gln
|
|
ENST00000286824.6:c.550G>C
|
ENSP00000286824.6:p.Glu184Gln
|
|
ENST00000378482.6:c.499G>C
|
ENSP00000367743.2:p.Glu167Gln
|
|
ENST00000419600.3:n.443G>C
|
|
|
ENST00000465127.1:c.589G>C
|
ENSP00000417050.1:p.Glu197Gln
|
|
ENST00000471410.5:c.*525G>C
|
ENSP00000419290.1:n.*525G>C
|
|
ENST00000475216.5:c.*492G>C
|
ENSP00000418586.1:n.*492G>C
|
|
ENST00000488893.5:n.682G>C
|
|
|
NM_004615.3:c.499G>C
|
NP_004606.2:p.Glu167Gln
|
|
NM_004615.4:c.499G>C
MANE Select
|
NP_004606.2:p.Glu167Gln
|
|