ENST00000682114.1:c.288A>C
|
ENSP00000507245.1:p.Glu96Asp
|
|
ENST00000682478.1:n.478A>C
|
|
|
ENST00000683576.1:n.478A>C
|
|
|
ENST00000683627.1:c.288A>C
|
ENSP00000507533.1:p.Glu96Asp
|
|
ENST00000684082.1:c.266-21A>C
|
ENSP00000508266.1:n.266-21A>C
|
|
ENST00000684633.1:n.260A>C
|
|
|
ENST00000684678.1:c.284A>C
|
ENSP00000507059.1:n.284A>C
|
|
ENST00000369842.9:c.288A>C
MANE Select
|
ENSP00000358857.4:p.Glu96Asp
|
|
ENST00000369835.3:c.183A>C
|
ENSP00000358850.3:p.Glu61Asp
|
|
ENST00000369842.8:c.288A>C
|
ENSP00000358857.4:p.Glu96Asp
|
|
ENST00000428228.5:c.*193A>C
|
ENSP00000401081.1:n.*193A>C
|
|
ENST00000468294.5:n.248A>C
|
|
|
ENST00000485261.1:n.478A>C
|
|
|
ENST00000486738.5:n.646A>C
|
|
|
ENST00000492448.1:n.271A>C
|
|
|
ENST00000494443.5:n.559A>C
|
|
|
NM_000117.2:c.288A>C , LRG_745t1:c.288A>C
|
NP_000108.1:p.Glu96Asp
|
|
XM_024452349.1:c.294A>C
|
XP_024308117.1:p.Glu98Asp
|
|
NM_000117.3:c.288A>C
MANE Select
|
NP_000108.1:p.Glu96Asp
|
|