ENST00000682114.1:c.408T>G
|
ENSP00000507245.1:p.Asp136Glu
|
|
ENST00000682478.1:n.598T>G
|
|
|
ENST00000683576.1:n.598T>G
|
|
|
ENST00000683627.1:c.408T>G
|
ENSP00000507533.1:p.Asp136Glu
|
|
ENST00000684082.1:c.365T>G
|
ENSP00000508266.1:n.365T>G
|
|
ENST00000684633.1:n.380T>G
|
|
|
ENST00000684678.1:c.404T>G
|
ENSP00000507059.1:n.404T>G
|
|
ENST00000369842.9:c.408T>G
MANE Select
|
ENSP00000358857.4:p.Asp136Glu
|
|
ENST00000369835.3:c.303T>G
|
ENSP00000358850.3:p.Asp101Glu
|
|
ENST00000369842.8:c.408T>G
|
ENSP00000358857.4:p.Asp136Glu
|
|
ENST00000428228.5:c.*313T>G
|
ENSP00000401081.1:n.*313T>G
|
|
ENST00000468294.5:n.368T>G
|
|
|
ENST00000471965.1:n.197T>G
|
|
|
ENST00000485261.1:n.598T>G
|
|
|
ENST00000486738.5:n.766T>G
|
|
|
ENST00000492448.1:n.391T>G
|
|
|
NM_000117.2:c.408T>G , LRG_745t1:c.408T>G
|
NP_000108.1:p.Asp136Glu
|
|
XM_024452349.1:c.414T>G
|
XP_024308117.1:p.Asp138Glu
|
|
NM_000117.3:c.408T>G
MANE Select
|
NP_000108.1:p.Asp136Glu
|
|