ENST00000628572.2:c.2966+37G>T
|
|
|
ENST00000637835.1:n.67+37G>T
|
|
|
ENST00000638043.2:c.4376+37G>T
|
ENSP00000490728.2:n.4376+37G>T
|
|
ENST00000642680.2:c.5036+37G>T
MANE Select
|
ENSP00000493871.2:n.5036+37G>T
|
|
ENST00000404807.5:c.5036+37G>T
|
ENSP00000384672.1:n.5036+37G>T
|
|
ENST00000407073.5:c.4337+37G>T
|
ENSP00000386049.1:n.4337+37G>T
|
|
ENST00000416015.2:c.3046+37G>T
|
|
|
ENST00000496893.3:n.2118+37G>T
|
|
|
ENST00000628572.1:c.576+37G>T
|
ENSP00000486209.1:n.576+37G>T
|
|
ENST00000629878.2:c.3243+37G>T
|
ENSP00000487089.1:n.3243+37G>T
|
|
ENST00000630352.1:c.162-10324G>T
|
|
|
NM_018328.4:c.4337+37G>T
|
NP_060798.2:n.4337+37G>T
|
|
XM_005263711.2:c.5036+37G>T
|
XP_005263768.1:n.5036+37G>T
|
|
XM_011511470.1:c.5075+37G>T
|
XP_011509772.1:n.5075+37G>T
|
|
XM_011511471.1:c.5075+37G>T
|
XP_011509773.1:n.5075+37G>T
|
|
XM_011511472.1:c.5075+37G>T
|
XP_011509774.1:n.5075+37G>T
|
|
XM_011511473.1:c.5075+37G>T
|
XP_011509775.1:n.5075+37G>T
|
|
XM_011511474.1:c.5036+37G>T
|
XP_011509776.1:n.5036+37G>T
|
|
XM_011511475.1:c.4376+37G>T
|
XP_011509777.1:n.4376+37G>T
|
|
XM_011511476.1:c.4337+37G>T
|
XP_011509778.1:n.4337+37G>T
|
|
XR_922967.1:n.6358+37G>T
|
|
|
XM_011511470.2:c.5075+37G>T
|
XP_011509772.1:n.5075+37G>T
|
|
XM_011511472.2:c.5075+37G>T
|
XP_011509774.1:n.5075+37G>T
|
|
XM_024452987.1:c.5036+37G>T
|
XP_024308755.1:n.5036+37G>T
|
|
XM_024452988.1:c.5075+37G>T
|
XP_024308756.1:n.5075+37G>T
|
|
XM_024452989.1:c.5036+37G>T
|
XP_024308757.1:n.5036+37G>T
|
|
XM_024452990.1:c.4376+37G>T
|
XP_024308758.1:n.4376+37G>T
|
|
XR_002959318.1:n.5441+37G>T
|
|
|
XR_002959319.1:n.4842+37G>T
|
|
|
NM_001378120.1:c.5036+37G>T
MANE Select
|
NP_001365049.1:n.5036+37G>T
|
|
NM_018328.5:c.4337+37G>T
|
NP_060798.2:n.4337+37G>T
|
|