ENST00000357578.8:c.487T>G
MANE Select
|
ENSP00000350191.3:p.Phe163Val
|
|
ENST00000672352.1:c.250T>G
|
ENSP00000500876.1:p.Phe84Val
|
|
ENST00000672557.1:c.405T>G
|
|
|
ENST00000672652.1:c.408T>G
|
|
|
ENST00000675422.1:n.1247T>G
|
|
|
ENST00000348925.2:c.487T>G
|
ENSP00000314649.3:p.Phe163Val
|
|
ENST00000357578.7:c.487T>G
|
ENSP00000350191.3:p.Phe163Val
|
|
ENST00000491546.5:c.403T>G
|
ENSP00000417687.1:p.Phe135Val
|
|
NM_001080.3:c.487T>G
MANE Select
|
NP_001071.1:p.Phe163Val
|
|
NM_170740.1:c.487T>G
|
NP_733936.1:p.Phe163Val
|
|
NM_001368954.1:c.487T>G
|
NP_001355883.1:p.Phe163Val
|
|