ENST00000262320.8:c.878+3683C>T
MANE Select
|
ENSP00000262320.3:n.878+3683C>T
|
|
ENST00000262320.7:c.878+3683C>T
|
ENSP00000262320.3:n.878+3683C>T
|
|
ENST00000354866.7:c.878+3683C>T
|
ENSP00000346935.3:n.878+3683C>T
|
|
ENST00000461023.5:n.175+3683C>T
|
|
|
ENST00000481769.1:n.305+9904C>T
|
|
|
NM_003502.3:c.878+3683C>T
|
NP_003493.1:n.878+3683C>T
|
|
NM_181050.2:c.878+3683C>T
|
NP_851393.1:n.878+3683C>T
|
|
XM_011522682.1:c.1025+3683C>T
|
XP_011520984.1:n.1025+3683C>T
|
|
XM_011522683.1:c.1025+3683C>T
|
XP_011520985.1:n.1025+3683C>T
|
|
XM_011522684.1:c.878+3683C>T
|
XP_011520986.1:n.878+3683C>T
|
|
XM_011522685.1:c.62+12593C>T
|
XP_011520987.1:n.62+12593C>T
|
|
XM_011522687.1:c.62+12593C>T
|
XP_011520989.1:n.62+12593C>T
|
|
XM_011522688.1:c.-1120+3683C>T
|
XP_011520990.1:n.-1120+3683C>T
|
|
NR_134879.1:n.1267+3683C>T
|
|
|
XM_011522682.2:c.1025+3683C>T
|
XP_011520984.1:n.1025+3683C>T
|
|
XM_011522683.2:c.1025+3683C>T
|
XP_011520985.1:n.1025+3683C>T
|
|
XM_011522684.2:c.878+3683C>T
|
XP_011520986.1:n.878+3683C>T
|
|
XM_017023743.1:c.1025+3683C>T
|
XP_016879232.1:n.1025+3683C>T
|
|
XM_017023744.1:c.1025+3683C>T
|
XP_016879233.1:n.1025+3683C>T
|
|
XM_017023747.1:c.1025+3683C>T
|
XP_016879236.1:n.1025+3683C>T
|
|
XM_017023748.1:c.1025+3683C>T
|
XP_016879237.1:n.1025+3683C>T
|
|
XR_001751996.1:n.1280+3683C>T
|
|
|
NM_003502.4:c.878+3683C>T
MANE Select
|
NP_003493.1:n.878+3683C>T
|
|
NM_181050.3:c.878+3683C>T
|
NP_851393.1:n.878+3683C>T
|
|
NR_134879.2:n.1314+3683C>T
|
|
|