ENST00000539966.6:c.597+772T>G
MANE Select
|
ENSP00000442539.2:n.597+772T>G
|
|
ENST00000376547.7:c.633+772T>G
|
ENSP00000365730.3:n.633+772T>G
|
|
ENST00000397517.6:c.540+772T>G
|
ENSP00000380651.3:n.540+772T>G
|
|
ENST00000444574.1:c.349+772T>G
|
|
|
ENST00000539966.5:c.597+772T>G
|
ENSP00000442539.2:n.597+772T>G
|
|
NM_001032296.3:c.597+772T>G
|
NP_001027467.2:n.597+772T>G
|
|
NM_001286649.1:c.540+772T>G
|
NP_001273578.1:n.540+772T>G
|
|
NM_003576.4:c.633+772T>G
|
NP_003567.2:n.633+772T>G
|
|
XM_005254078.3:c.303+772T>G
|
XP_005254135.1:n.303+772T>G
|
|
XM_005254079.3:c.303+772T>G
|
XP_005254136.1:n.303+772T>G
|
|
XM_005254079.5:c.303+772T>G
|
XP_005254136.1:n.303+772T>G
|
|
XM_017020794.2:c.855+772T>G
|
XP_016876283.1:n.855+772T>G
|
|
XM_024449426.1:c.303+772T>G
|
XP_024305194.1:n.303+772T>G
|
|
NM_001032296.4:c.597+772T>G
MANE Select
|
NP_001027467.2:n.597+772T>G
|
|
NM_001286649.2:c.540+772T>G
|
NP_001273578.1:n.540+772T>G
|
|
NM_003576.5:c.633+772T>G
|
NP_003567.2:n.633+772T>G
|
|