ENST00000298910.12:c.237+1378G>T
MANE Select
|
ENSP00000298910.7:n.237+1378G>T
|
|
ENST00000644108.1:c.182-873G>T
|
|
|
ENST00000679360.1:c.237+1378G>T
|
ENSP00000505368.1:n.237+1378G>T
|
|
ENST00000680235.1:n.392+1378G>T
|
|
|
ENST00000680790.1:c.237+1378G>T
|
ENSP00000505335.1:n.237+1378G>T
|
|
ENST00000298910.11:c.237+1378G>T
|
ENSP00000298910.7:n.237+1378G>T
|
|
ENST00000343742.6:c.237+1378G>T
|
ENSP00000341930.2:n.237+1378G>T
|
|
ENST00000416796.5:c.24+1378G>T
|
ENSP00000398726.1:n.24+1378G>T
|
|
ENST00000474202.1:n.46+1378G>T
|
|
|
NM_198578.3:c.237+1378G>T
|
NP_940980.3:n.237+1378G>T
|
|
XM_005268629.2:c.237+1378G>T
|
XP_005268686.1:n.237+1378G>T
|
|
XM_011537877.1:c.237+1378G>T
|
XP_011536179.1:n.237+1378G>T
|
|
XM_011537878.1:c.237+1378G>T
|
XP_011536180.1:n.237+1378G>T
|
|
XM_011537880.1:c.237+1378G>T
|
XP_011536182.1:n.237+1378G>T
|
|
XM_011537881.1:c.237+1378G>T
|
XP_011536183.1:n.237+1378G>T
|
|
XM_011537882.1:c.237+1378G>T
|
XP_011536184.1:n.237+1378G>T
|
|
XM_005268629.4:c.237+1378G>T
|
XP_005268686.1:n.237+1378G>T
|
|
XM_011537877.3:c.237+1378G>T
|
XP_011536179.1:n.237+1378G>T
|
|
XM_011537881.3:c.237+1378G>T
|
XP_011536183.1:n.237+1378G>T
|
|
XM_011537882.3:c.237+1378G>T
|
XP_011536184.1:n.237+1378G>T
|
|
XM_017018786.2:c.237+1378G>T
|
XP_016874275.1:n.237+1378G>T
|
|
XM_017018789.2:c.237+1378G>T
|
XP_016874278.1:n.237+1378G>T
|
|
XR_001748574.2:n.479+1378G>T
|
|
|
NM_198578.4:c.237+1378G>T
MANE Select
|
NP_940980.4:n.237+1378G>T
|
|