ENST00000682012.1:n.795+255G>T
|
|
|
ENST00000684569.1:n.651+255G>T
|
|
|
ENST00000561421.6:c.606+255G>T
MANE Select
|
ENSP00000453347.2:n.606+255G>T
|
|
ENST00000646551.1:n.2233+255G>T
|
|
|
ENST00000261755.9:c.606+255G>T
|
ENSP00000261755.5:n.606+255G>T
|
|
ENST00000407106.5:c.606+255G>T
|
ENSP00000385080.1:n.606+255G>T
|
|
ENST00000539156.5:c.396+255G>T
|
ENSP00000454271.1:n.396+255G>T
|
|
ENST00000558627.1:n.534+255G>T
|
|
|
ENST00000561421.5:c.606+255G>T
|
ENSP00000453347.1:n.606+255G>T
|
|
NM_000137.2:c.606+255G>T
|
NP_000128.1:n.606+255G>T
|
|
XM_024449872.1:c.606+255G>T
|
XP_024305640.1:n.606+255G>T
|
|
NM_000137.4:c.606+255G>T
MANE Select
|
NP_000128.1:n.606+255G>T
|
|
NM_001374377.1:c.606+255G>T
|
NP_001361306.1:n.606+255G>T
|
|
NM_001374380.1:c.606+255G>T
|
NP_001361309.1:n.606+255G>T
|
|