ENST00000682114.1:c.225T>C
|
ENSP00000507245.1:p.Asp75=
|
|
ENST00000682478.1:n.201T>C
|
|
|
ENST00000683576.1:n.201T>C
|
|
|
ENST00000683627.1:c.225T>C
|
ENSP00000507533.1:p.Asp75=
|
|
ENST00000684082.1:c.225T>C
|
ENSP00000508266.1:p.Asp75=
|
|
ENST00000684633.1:n.197T>C
|
|
|
ENST00000684678.1:c.221T>C
|
ENSP00000507059.1:n.221T>C
|
|
ENST00000369842.9:c.225T>C
MANE Select
|
ENSP00000358857.4:p.Asp75=
|
|
ENST00000369835.3:c.120T>C
|
ENSP00000358850.3:p.Asp40=
|
|
ENST00000369842.8:c.225T>C
|
ENSP00000358857.4:p.Asp75=
|
|
ENST00000428228.5:c.*130T>C
|
ENSP00000401081.1:n.*130T>C
|
|
ENST00000468294.5:n.185T>C
|
|
|
ENST00000485261.1:n.201T>C
|
|
|
ENST00000486738.5:n.369T>C
|
|
|
ENST00000492448.1:n.208T>C
|
|
|
ENST00000494443.5:n.282T>C
|
|
|
NM_000117.2:c.225T>C , LRG_745t1:c.225T>C
|
NP_000108.1:p.Asp75=
|
|
XM_024452349.1:c.17T>C
|
XP_024308117.1:p.Ile6Thr
|
|
NM_000117.3:c.225T>C
MANE Select
|
NP_000108.1:p.Asp75=
|
|