ENST00000682153.1:c.8867+126T>C
|
ENSP00000507923.1:n.8867+126T>C
|
|
ENST00000682358.1:n.8937+126T>C
|
|
|
ENST00000683334.1:c.*4549+126T>C
|
ENSP00000507369.1:n.*4549+126T>C
|
|
ENST00000357162.7:c.8792+126T>C
MANE Select
|
ENSP00000349685.2:n.8792+126T>C
|
|
ENST00000358544.7:c.8867+126T>C
MANE Plus Clinical
|
ENSP00000351346.2:n.8867+126T>C
|
|
ENST00000357162.6:c.8792+126T>C
|
ENSP00000349685.2:n.8792+126T>C
|
|
ENST00000358544.6:c.8867+126T>C
|
ENSP00000351346.2:n.8867+126T>C
|
|
NM_017890.4:c.8867+126T>C , LRG_351t1:c.8867+126T>C
|
NP_060360.3:n.8867+126T>C
|
|
NM_152564.4:c.8792+126T>C , LRG_351t2:c.8792+126T>C
|
NP_689777.3:n.8792+126T>C
|
|
XM_005250800.2:c.8867+126T>C
|
XP_005250857.1:n.8867+126T>C
|
|
XM_005250801.3:c.8867+126T>C
|
XP_005250858.1:n.8867+126T>C
|
|
XM_011516848.1:c.8864+126T>C
|
XP_011515150.1:n.8864+126T>C
|
|
XM_011516849.1:c.8789+126T>C
|
XP_011515151.1:n.8789+126T>C
|
|
XM_011516850.1:c.8489+126T>C
|
XP_011515152.1:n.8489+126T>C
|
|
XM_011516851.1:c.5753+126T>C
|
XP_011515153.1:n.5753+126T>C
|
|
XM_011516852.1:c.5753+126T>C
|
XP_011515154.1:n.5753+126T>C
|
|
XM_011516854.1:c.4646+126T>C
|
XP_011515156.1:n.4646+126T>C
|
|
XM_005250800.3:c.8867+126T>C
|
XP_005250857.1:n.8867+126T>C
|
|
XM_005250801.5:c.8867+126T>C
|
XP_005250858.1:n.8867+126T>C
|
|
XM_011516848.2:c.8864+126T>C
|
XP_011515150.1:n.8864+126T>C
|
|
XM_011516849.2:c.8789+126T>C
|
XP_011515151.1:n.8789+126T>C
|
|
XM_011516850.2:c.8489+126T>C
|
XP_011515152.1:n.8489+126T>C
|
|
XM_011516851.2:c.5753+126T>C
|
XP_011515153.1:n.5753+126T>C
|
|
XM_011516852.2:c.5753+126T>C
|
XP_011515154.1:n.5753+126T>C
|
|
XM_011516854.2:c.4646+126T>C
|
XP_011515156.1:n.4646+126T>C
|
|
XM_017013109.1:c.8672+126T>C
|
XP_016868598.1:n.8672+126T>C
|
|
XM_017013111.1:c.5753+126T>C
|
XP_016868600.1:n.5753+126T>C
|
|
XM_017013112.1:c.4424+126T>C
|
XP_016868601.1:n.4424+126T>C
|
|
XM_024447074.1:c.7652+126T>C
|
XP_024302842.1:n.7652+126T>C
|
|
NM_017890.5:c.8867+126T>C
MANE Plus Clinical
|
NP_060360.3:n.8867+126T>C
|
|
NM_152564.5:c.8792+126T>C
MANE Select
|
NP_689777.3:n.8792+126T>C
|
|