ENST00000434651.7:c.127T>G
MANE Select
|
ENSP00000407332.2:p.Phe43Val
|
|
ENST00000374943.8:c.127T>G
|
ENSP00000364080.4:p.Phe43Val
|
|
ENST00000399079.7:c.127T>G
|
ENSP00000382029.3:p.Phe43Val
|
|
ENST00000399082.7:c.109+1449T>G
|
ENSP00000382032.3:n.109+1449T>G
|
|
ENST00000399084.5:c.127T>G
|
ENSP00000382034.1:p.Phe43Val
|
|
ENST00000434651.6:c.127T>G
|
ENSP00000407332.2:p.Phe43Val
|
|
ENST00000484729.2:c.127T>G
|
ENSP00000436686.1:p.Phe43Val
|
|
ENST00000487676.1:n.158T>G
|
|
|
NM_001243961.1:c.127T>G
|
NP_001230890.1:p.Phe43Val
|
|
NM_002123.4:c.127T>G
|
NP_002114.3:p.Phe43Val
|
|
NM_001243961.2:c.127T>G
|
NP_001230890.1:p.Phe43Val
|
|
NM_002123.5:c.127T>G
MANE Select
|
NP_002114.3:p.Phe43Val
|
|