|
NM_001080.3:c.698C>T
MANE Select
|
NP_001071.1:p.Thr233Met
|
|
ENST00000357578.8:c.698C>T
MANE Select
|
ENSP00000350191.3:p.Thr233Met
|
|
NM_001368954.1:c.698C>T
|
NP_001355883.1:p.Thr233Met
|
|
NM_170740.1:c.698C>T
|
NP_733936.1:p.Thr233Met
|
|
ENST00000348925.2:c.698C>T
|
ENSP00000314649.3:p.Thr233Met
|
|
ENST00000357578.7:c.698C>T
|
ENSP00000350191.3:p.Thr233Met
|
|
ENST00000491546.5:c.614C>T
|
ENSP00000417687.1:p.Thr205Met
|
|
ENST00000672352.1:c.461C>T
|
ENSP00000500876.1:p.Thr154Met
|
|
ENST00000672557.1:c.616C>T
|
|
|
ENST00000672619.1:n.58C>T
|
|
|
ENST00000672652.1:c.619C>T
|
|
|
ENST00000675422.1:n.1458C>T
|
|