ENST00000682114.1:c.265+12G>C
|
ENSP00000507245.1:n.265+12G>C
|
|
ENST00000682478.1:n.253G>C
|
|
|
ENST00000683576.1:n.253G>C
|
|
|
ENST00000683627.1:c.265+12G>C
|
ENSP00000507533.1:n.265+12G>C
|
|
ENST00000684082.1:c.265+12G>C
|
ENSP00000508266.1:n.265+12G>C
|
|
ENST00000684633.1:n.237+12G>C
|
|
|
ENST00000684678.1:c.261+12G>C
|
ENSP00000507059.1:n.261+12G>C
|
|
ENST00000369842.9:c.265+12G>C
MANE Select
|
ENSP00000358857.4:n.265+12G>C
|
|
ENST00000369835.3:c.160+12G>C
|
ENSP00000358850.3:n.160+12G>C
|
|
ENST00000369842.8:c.265+12G>C
|
ENSP00000358857.4:n.265+12G>C
|
|
ENST00000428228.5:c.*170+12G>C
|
ENSP00000401081.1:n.*170+12G>C
|
|
ENST00000468294.5:n.225+12G>C
|
|
|
ENST00000485261.1:n.253G>C
|
|
|
ENST00000486738.5:n.421G>C
|
|
|
ENST00000492448.1:n.248+12G>C
|
|
|
ENST00000494443.5:n.334G>C
|
|
|
NM_000117.2:c.265+12G>C , LRG_745t1:c.265+12G>C
|
NP_000108.1:n.265+12G>C
|
|
XM_024452349.1:c.69G>C
|
XP_024308117.1:p.Gly23=
|
|
NM_000117.3:c.265+12G>C
MANE Select
|
NP_000108.1:n.265+12G>C
|
|