ENST00000561514.3:c.-676G>T
|
ENSP00000460666.3:n.-676G>T
|
|
ENST00000565038.2:c.48+129G>T
|
ENSP00000459882.2:n.48+129G>T
|
|
ENST00000566069.6:c.48+129G>T
|
ENSP00000459237.2:n.48+129G>T
|
|
ENST00000697377.2:c.-192+129G>T
|
ENSP00000513286.2:n.-192+129G>T
|
|
ENST00000697379.2:c.-98+129G>T
|
ENSP00000513287.2:n.-98+129G>T
|
|
ENST00000561514.2:c.-1567G>T
|
ENSP00000460666.2:n.-1567G>T
|
|
ENST00000697374.1:c.-1158G>T
|
ENSP00000513284.1:n.-1158G>T
|
|
ENST00000697376.1:c.-1008+129G>T
|
ENSP00000513285.1:n.-1008+129G>T
|
|
ENST00000697377.1:c.-1083+129G>T
|
ENSP00000513286.1:n.-1083+129G>T
|
|
ENST00000697379.1:c.-989+129G>T
|
ENSP00000513287.1:n.-989+129G>T
|
|
ENST00000697382.1:c.-1618G>T
|
ENSP00000513288.1:n.-1618G>T
|
|
ENST00000697383.1:c.48+129G>T
|
ENSP00000513289.1:n.48+129G>T
|
|
ENST00000697384.1:n.202+129G>T
|
|
|
ENST00000261584.9:c.48+129G>T
MANE Select
|
ENSP00000261584.4:n.48+129G>T
|
|
ENST00000261584.8:c.48+129G>T
|
ENSP00000261584.4:n.48+129G>T
|
|
ENST00000567003.1:n.192+129G>T
|
|
|
ENST00000568219.5:c.-838+146G>T
|
ENSP00000454703.2:n.-838+146G>T
|
|
NM_024675.3:c.48+129G>T , LRG_308t1:c.48+129G>T
|
NP_078951.2:n.48+129G>T
|
|
XM_011545946.1:c.-676G>T
|
XP_011544248.1:n.-676G>T
|
|
XM_011545947.1:c.-676G>T
|
XP_011544249.1:n.-676G>T
|
|
XM_011545948.1:c.-972+129G>T
|
XP_011544250.1:n.-972+129G>T
|
|
XR_950851.1:n.115G>T
|
|
|
XM_011545946.2:c.-676G>T
|
XP_011544248.1:n.-676G>T
|
|
XM_011545947.2:c.-676G>T
|
XP_011544249.1:n.-676G>T
|
|
XM_011545948.2:c.-972+129G>T
|
XP_011544250.1:n.-972+129G>T
|
|
XM_017023671.1:c.-676G>T
|
XP_016879160.1:n.-676G>T
|
|
XM_017023672.2:c.48+129G>T
|
XP_016879161.1:n.48+129G>T
|
|
XM_017023673.2:c.48+129G>T
|
XP_016879162.1:n.48+129G>T
|
|
NM_024675.4:c.48+129G>T
MANE Select
|
NP_078951.2:n.48+129G>T
|
|