ENST00000682114.1:c.449+2T>G
|
ENSP00000507245.1:n.449+2T>G
|
|
ENST00000682478.1:n.639+2T>G
|
|
|
ENST00000683576.1:n.639+2T>G
|
|
|
ENST00000683627.1:c.449+2T>G
|
ENSP00000507533.1:n.449+2T>G
|
|
ENST00000684082.1:c.406+2T>G
|
ENSP00000508266.1:n.406+2T>G
|
|
ENST00000684633.1:n.421+2T>G
|
|
|
ENST00000684678.1:c.445+2T>G
|
ENSP00000507059.1:n.445+2T>G
|
|
ENST00000369842.9:c.449+2T>G
MANE Select
|
ENSP00000358857.4:n.449+2T>G
|
|
ENST00000369835.3:c.344+2T>G
|
ENSP00000358850.3:n.344+2T>G
|
|
ENST00000369842.8:c.449+2T>G
|
ENSP00000358857.4:n.449+2T>G
|
|
ENST00000428228.5:c.*354+2T>G
|
ENSP00000401081.1:n.*354+2T>G
|
|
ENST00000468294.5:n.411T>G
|
|
|
ENST00000471965.1:n.238+2T>G
|
|
|
ENST00000485261.1:n.641T>G
|
|
|
ENST00000486738.5:n.809T>G
|
|
|
ENST00000492448.1:n.432+2T>G
|
|
|
NM_000117.2:c.449+2T>G , LRG_745t1:c.449+2T>G
|
NP_000108.1:n.449+2T>G
|
|
XM_024452349.1:c.455+2T>G
|
XP_024308117.1:n.455+2T>G
|
|
NM_000117.3:c.449+2T>G
MANE Select
|
NP_000108.1:n.449+2T>G
|
|