ENST00000491889.6:c.-98-943T>G
|
ENSP00000419914.1:n.-98-943T>G
|
|
ENST00000682749.1:c.-78+11955T>G
|
ENSP00000507306.1:n.-78+11955T>G
|
|
ENST00000381971.8:c.-98-943T>G
MANE Select
|
ENSP00000371398.3:n.-98-943T>G
|
|
ENST00000381971.7:c.-98-943T>G
|
ENSP00000371398.3:n.-98-943T>G
|
|
ENST00000465708.5:n.497-943T>G
|
|
|
ENST00000471664.1:n.585-943T>G
|
|
|
ENST00000477901.5:c.-98-943T>G
|
ENSP00000417794.1:n.-98-943T>G
|
|
ENST00000478844.5:c.-78+10918T>G
|
ENSP00000418005.1:n.-78+10918T>G
|
|
ENST00000481827.5:c.-98-943T>G
|
ENSP00000417883.1:n.-98-943T>G
|
|
ENST00000490709.1:n.416+11955T>G
|
|
|
ENST00000491889.5:c.-98-943T>G
|
ENSP00000419914.1:n.-98-943T>G
|
|
NM_001042413.1:c.-98-943T>G
|
NP_001035878.1:n.-98-943T>G
|
|
XM_005251386.3:c.-78+11955T>G
|
XP_005251443.1:n.-78+11955T>G
|
|
XM_005251387.3:c.-556-943T>G
|
XP_005251444.1:n.-556-943T>G
|
|
XM_005251388.3:c.-71+11955T>G
|
XP_005251445.1:n.-71+11955T>G
|
|
XM_005251389.3:c.-98-943T>G
|
XP_005251446.1:n.-98-943T>G
|
|
XM_006716731.2:c.-98-943T>G
|
XP_006716794.1:n.-98-943T>G
|
|
XM_011517763.1:c.-98-943T>G
|
XP_011516065.1:n.-98-943T>G
|
|
XM_011517764.1:c.-98-943T>G
|
XP_011516066.1:n.-98-943T>G
|
|
XM_011517765.1:c.-98-943T>G
|
XP_011516067.1:n.-98-943T>G
|
|
XM_011517767.1:c.-556-943T>G
|
XP_011516069.1:n.-556-943T>G
|
|
XM_011517768.1:c.-98-943T>G
|
XP_011516070.1:n.-98-943T>G
|
|
XM_011517769.1:c.-98-943T>G
|
XP_011516071.1:n.-98-943T>G
|
|
XR_929206.1:n.669-943T>G
|
|
|
XM_005251386.4:c.-78+11955T>G
|
XP_005251443.1:n.-78+11955T>G
|
|
XM_005251387.4:c.-556-943T>G
|
XP_005251444.1:n.-556-943T>G
|
|
XM_005251388.4:c.-71+11955T>G
|
XP_005251445.1:n.-71+11955T>G
|
|
XM_005251389.5:c.-98-943T>G
|
XP_005251446.1:n.-98-943T>G
|
|
XM_006716731.3:c.-98-943T>G
|
XP_006716794.1:n.-98-943T>G
|
|
XM_011517763.2:c.-98-943T>G
|
XP_011516065.1:n.-98-943T>G
|
|
XM_011517764.2:c.-98-943T>G
|
XP_011516066.1:n.-98-943T>G
|
|
XM_011517765.2:c.-98-943T>G
|
XP_011516067.1:n.-98-943T>G
|
|
XM_011517767.3:c.-556-943T>G
|
XP_011516069.1:n.-556-943T>G
|
|
XM_011517769.2:c.-98-943T>G
|
XP_011516071.1:n.-98-943T>G
|
|
XR_929206.2:n.665-943T>G
|
|
|
NM_001042413.2:c.-98-943T>G
MANE Select
|
NP_001035878.1:n.-98-943T>G
|
|