ENST00000216927.4:c.749-389G>T
|
ENSP00000216927.4:n.749-389G>T
|
|
ENST00000303415.7:c.1082-389G>T
MANE Select
|
ENSP00000305529.3:n.1082-389G>T
|
|
ENST00000344103.8:c.431-389G>T
|
ENSP00000342759.4:n.431-389G>T
|
|
ENST00000381580.5:c.983-389G>T
|
ENSP00000370992.1:n.983-389G>T
|
|
ENST00000381583.6:c.749-389G>T
|
ENSP00000370995.2:n.749-389G>T
|
|
ENST00000478145.6:n.142G>T
|
|
|
NM_001039508.1:c.749-389G>T
|
NP_001034597.1:n.749-389G>T
|
|
NM_018556.3:c.1082-389G>T
|
NP_061026.2:n.1082-389G>T
|
|
NM_080816.2:c.431-389G>T
|
NP_543006.2:n.431-389G>T
|
|
XM_005260749.2:c.764-389G>T
|
XP_005260806.1:n.764-389G>T
|
|
XM_011529286.1:c.983-389G>T
|
XP_011527588.1:n.983-389G>T
|
|
XM_005260749.4:c.764-389G>T
|
XP_005260806.1:n.764-389G>T
|
|
XM_011529286.2:c.983-389G>T
|
XP_011527588.1:n.983-389G>T
|
|
NM_018556.4:c.1082-389G>T
MANE Select
|
NP_061026.2:n.1082-389G>T
|
|
NM_080816.3:c.431-389G>T
|
NP_543006.2:n.431-389G>T
|
|
NM_001039508.2:c.749-389G>T
|
NP_001034597.1:n.749-389G>T
|
|