ENST00000393716.8:c.190T>G
MANE Select
|
ENSP00000377319.3:p.Phe64Val
|
|
ENST00000466380.6:c.190T>G
|
ENSP00000420297.2:p.Phe64Val
|
|
ENST00000648112.1:c.*213T>G
|
ENSP00000497876.1:n.*213T>G
|
|
ENST00000337940.4:c.307T>G
|
ENSP00000336528.4:p.Phe103Val
|
|
ENST00000393716.6:c.190T>G
|
ENSP00000377319.2:p.Phe64Val
|
|
ENST00000466380.5:c.190T>G
|
ENSP00000420297.1:p.Phe64Val
|
|
ENST00000474090.1:n.478T>G
|
|
|
NM_003889.3:c.190T>G
|
NP_003880.3:p.Phe64Val
|
|
NM_022002.2:c.307T>G
|
NP_071285.1:p.Phe103Val
|
|
NM_033013.2:c.190T>G
|
NP_148934.1:p.Phe64Val
|
|
NM_003889.4:c.190T>G
MANE Select
|
NP_003880.3:p.Phe64Val
|
|
NM_022002.3:c.307T>G
|
NP_071285.1:p.Phe103Val
|
|
NM_033013.3:c.190T>G
|
NP_148934.1:p.Phe64Val
|
|