|
ENST00000317173.9:c.142+74487G>C
MANE Select
|
ENSP00000313921.4:n.142+74487G>C
|
|
|
ENST00000317173.8:c.142+74487G>C
|
ENSP00000313921.4:n.142+74487G>C
|
|
|
ENST00000382490.9:c.13+33102G>C
|
ENSP00000371930.5:n.13+33102G>C
|
|
|
ENST00000441698.6:c.142+74487G>C
|
ENSP00000410912.2:n.142+74487G>C
|
|
|
ENST00000518255.5:c.142+74487G>C
|
ENSP00000429461.1:n.142+74487G>C
|
|
|
ENST00000521209.6:c.-57+70046G>C
|
ENSP00000435644.1:n.-57+70046G>C
|
|
|
ENST00000522907.5:c.-57+32827G>C
|
ENSP00000428214.1:n.-57+32827G>C
|
|
|
ENST00000523637.2:n.317+33102G>C
|
|
|
|
ENST00000528246.5:c.-57+32827G>C
|
ENSP00000436839.1:n.-57+32827G>C
|
|
|
NM_001135670.2:c.142+74487G>C
|
NP_001129142.1:n.142+74487G>C
|
|
|
NM_001135671.2:c.13+33102G>C
|
NP_001129143.1:n.13+33102G>C
|
|
|
NM_001199729.2:c.-57+32827G>C
|
NP_001186658.1:n.-57+32827G>C
|
|
|
NM_012331.4:c.142+74487G>C
|
NP_036463.1:n.142+74487G>C
|
|
|
XM_011543822.1:c.142+74487G>C
|
XP_011542124.1:n.142+74487G>C
|
|
|
XM_011543823.1:c.142+74487G>C
|
XP_011542125.1:n.142+74487G>C
|
|
|
XM_011543822.2:c.142+74487G>C
|
XP_011542124.1:n.142+74487G>C
|
|
|
XM_011543823.2:c.142+74487G>C
|
XP_011542125.1:n.142+74487G>C
|
|
|
XM_017013448.2:c.142+74487G>C
|
XP_016868937.1:n.142+74487G>C
|
|
|
XM_017013449.2:c.-57+32827G>C
|
XP_016868938.1:n.-57+32827G>C
|
|
|
XM_017013450.2:c.-57+32622G>C
|
XP_016868939.1:n.-57+32622G>C
|
|
|
XM_017013451.2:c.13+33102G>C
|
XP_016868940.1:n.13+33102G>C
|
|
|
XM_024447162.1:c.142+74487G>C
|
XP_024302930.1:n.142+74487G>C
|
|
|
NM_012331.5:c.142+74487G>C
MANE Select
|
NP_036463.1:n.142+74487G>C
|
|
|
NM_001135670.3:c.142+74487G>C
|
NP_001129142.1:n.142+74487G>C
|
|
|
NM_001135671.3:c.13+33102G>C
|
NP_001129143.1:n.13+33102G>C
|
|
|
NM_001199729.3:c.-57+32827G>C
|
NP_001186658.1:n.-57+32827G>C
|
|
