ENST00000341119.10:c.824-676C>G
MANE Select
|
ENSP00000344831.5:n.824-676C>G
|
|
ENST00000341119.9:c.824-676C>G
|
ENSP00000344831.5:n.824-676C>G
|
|
ENST00000429674.5:c.*641-676C>G
|
ENSP00000405566.1:n.*641-676C>G
|
|
ENST00000446236.5:c.*187-676C>G
|
ENSP00000401473.1:n.*187-676C>G
|
|
ENST00000470328.1:n.636-1125C>G
|
|
|
ENST00000496348.5:n.110-676C>G
|
|
|
NM_018843.3:c.824-676C>G
|
NP_061331.2:n.824-676C>G
|
|
XM_005250496.3:c.824-676C>G
|
XP_005250553.1:n.824-676C>G
|
|
XM_011516401.1:c.824-676C>G
|
XP_011514703.1:n.824-676C>G
|
|
XM_011516402.1:c.824-676C>G
|
XP_011514704.1:n.824-676C>G
|
|
XM_011516403.1:c.824-1125C>G
|
XP_011514705.1:n.824-1125C>G
|
|
XM_011516404.1:c.638-676C>G
|
XP_011514706.1:n.638-676C>G
|
|
XM_011516405.1:c.638-676C>G
|
XP_011514707.1:n.638-676C>G
|
|
XR_927490.1:n.1300-676C>G
|
|
|
NM_018843.4:c.824-676C>G
MANE Select
|
NP_061331.2:n.824-676C>G
|
|