ENST00000682114.1:c.266-71T>C
|
ENSP00000507245.1:n.266-71T>C
|
|
ENST00000682478.1:n.385T>C
|
|
|
ENST00000683576.1:n.385T>C
|
|
|
ENST00000683627.1:c.266-71T>C
|
ENSP00000507533.1:n.266-71T>C
|
|
ENST00000684082.1:c.266-114T>C
|
ENSP00000508266.1:n.266-114T>C
|
|
ENST00000684633.1:n.238-71T>C
|
|
|
ENST00000684678.1:c.262-71T>C
|
ENSP00000507059.1:n.262-71T>C
|
|
ENST00000369842.9:c.266-71T>C
MANE Select
|
ENSP00000358857.4:n.266-71T>C
|
|
ENST00000369835.3:c.161-71T>C
|
ENSP00000358850.3:n.161-71T>C
|
|
ENST00000369842.8:c.266-71T>C
|
ENSP00000358857.4:n.266-71T>C
|
|
ENST00000428228.5:c.*171-71T>C
|
ENSP00000401081.1:n.*171-71T>C
|
|
ENST00000468294.5:n.226-71T>C
|
|
|
ENST00000485261.1:n.385T>C
|
|
|
ENST00000486738.5:n.553T>C
|
|
|
ENST00000492448.1:n.249-71T>C
|
|
|
ENST00000494443.5:n.466T>C
|
|
|
NM_000117.2:c.266-71T>C , LRG_745t1:c.266-71T>C
|
NP_000108.1:n.266-71T>C
|
|
XM_024452349.1:c.201T>C
|
XP_024308117.1:p.Ile67=
|
|
NM_000117.3:c.266-71T>C
MANE Select
|
NP_000108.1:n.266-71T>C
|
|