|
NM_032119.4:c.11581-2A>G
MANE Select
|
NP_115495.3:n.11581-2A>G
|
|
ENST00000405460.9:c.11581-2A>G
MANE Select
|
ENSP00000384582.2:n.11581-2A>G
|
|
NM_032119.3:c.11581-2A>G
|
NP_115495.3:n.11581-2A>G
|
|
NR_003149.1:n.11594-2A>G
|
|
|
NR_003149.2:n.11597-2A>G
|
|
|
ENST00000405460.6:c.11581-2A>G
|
ENSP00000384582.2:n.11581-2A>G
|
|
ENST00000425867.3:c.712-527A>G
|
ENSP00000392618.3:n.712-527A>G
|
|
ENST00000509621.1:c.4278-2A>G
|
|
|
ENST00000639431.1:c.265+80243A>G
|
ENSP00000491057.1:n.265+80243A>G
|
|
ENST00000640374.1:n.4725-527A>G
|
|
|
ENST00000640464.1:n.2000-2A>G
|
|
|
XM_011543675.1:c.11578-2A>G
|
XP_011541977.1:n.11578-2A>G
|
|
XM_011543676.1:c.11500-2A>G
|
XP_011541978.1:n.11500-2A>G
|
|
XM_011543677.1:c.8884-2A>G
|
XP_011541979.1:n.8884-2A>G
|
|
XM_011543678.1:c.11581-2A>G
|
XP_011541980.1:n.11581-2A>G
|
|
XM_017009963.2:c.11602-2A>G
|
XP_016865452.1:n.11602-2A>G
|
|
XM_017009964.2:c.11599-2A>G
|
XP_016865453.1:n.11599-2A>G
|
|
XM_017009965.1:c.11599-2A>G
|
XP_016865454.1:n.11599-2A>G
|
|
XM_017009966.2:c.11521-2A>G
|
XP_016865455.1:n.11521-2A>G
|
|
XM_017009967.1:c.11506-2A>G
|
XP_016865456.1:n.11506-2A>G
|
|
XM_017009968.2:c.11602-2A>G
|
XP_016865457.1:n.11602-2A>G
|
|
XM_017009969.2:c.11602-2A>G
|
XP_016865458.1:n.11602-2A>G
|
|
XM_017009970.2:c.11602-2A>G
|
XP_016865459.1:n.11602-2A>G
|
|
XM_017009971.2:c.11602-2A>G
|
XP_016865460.1:n.11602-2A>G
|
|
XM_017009972.1:c.4720-2A>G
|
XP_016865461.1:n.4720-2A>G
|
|
XM_017009973.1:c.4699-2A>G
|
XP_016865462.1:n.4699-2A>G
|