ENST00000341048.9:c.484-4927C>T
MANE Select
|
ENSP00000342295.4:n.484-4927C>T
|
|
ENST00000341048.8:c.484-4927C>T
|
ENSP00000342295.4:n.484-4927C>T
|
|
ENST00000504958.6:c.483+10977C>T
|
ENSP00000424230.1:n.483+10977C>T
|
|
ENST00000505970.2:n.254-4927C>T
|
|
|
ENST00000513241.2:c.397-4927C>T
|
ENSP00000423507.2:n.397-4927C>T
|
|
NM_024669.2:c.484-4927C>T
|
NP_078945.2:n.484-4927C>T
|
|
XM_006714691.2:c.-3-4927C>T
|
XP_006714754.1:n.-3-4927C>T
|
|
XM_017009852.1:c.484-4927C>T
|
XP_016865341.1:n.484-4927C>T
|
|
XM_017009853.1:c.484-4927C>T
|
XP_016865342.1:n.484-4927C>T
|
|
XM_017009854.1:c.-3-4927C>T
|
XP_016865343.1:n.-3-4927C>T
|
|
NM_024669.3:c.484-4927C>T
MANE Select
|
NP_078945.2:n.484-4927C>T
|
|