|
ENST00000405460.9:c.11122-2A>G
MANE Select
|
ENSP00000384582.2:n.11122-2A>G
|
|
|
ENST00000425867.3:c.253-2A>G
|
ENSP00000392618.3:n.253-2A>G
|
|
|
ENST00000639431.1:c.265+77363A>G
|
ENSP00000491057.1:n.265+77363A>G
|
|
|
ENST00000640374.1:n.4266-2A>G
|
|
|
|
ENST00000640464.1:n.1541-2A>G
|
|
|
|
ENST00000405460.6:c.11122-2A>G
|
ENSP00000384582.2:n.11122-2A>G
|
|
|
ENST00000509621.1:c.3819-2A>G
|
|
|
|
NM_032119.3:c.11122-2A>G
|
NP_115495.3:n.11122-2A>G
|
|
|
NR_003149.1:n.11135-2A>G
|
|
|
|
XM_011543675.1:c.11119-2A>G
|
XP_011541977.1:n.11119-2A>G
|
|
|
XM_011543676.1:c.11041-2A>G
|
XP_011541978.1:n.11041-2A>G
|
|
|
XM_011543677.1:c.8425-2A>G
|
XP_011541979.1:n.8425-2A>G
|
|
|
XM_011543678.1:c.11122-2A>G
|
XP_011541980.1:n.11122-2A>G
|
|
|
NM_032119.4:c.11122-2A>G
MANE Select
|
NP_115495.3:n.11122-2A>G
|
|
|
XM_017009963.2:c.11143-2A>G
|
XP_016865452.1:n.11143-2A>G
|
|
|
XM_017009964.2:c.11140-2A>G
|
XP_016865453.1:n.11140-2A>G
|
|
|
XM_017009965.1:c.11140-2A>G
|
XP_016865454.1:n.11140-2A>G
|
|
|
XM_017009966.2:c.11062-2A>G
|
XP_016865455.1:n.11062-2A>G
|
|
|
XM_017009967.1:c.11047-2A>G
|
XP_016865456.1:n.11047-2A>G
|
|
|
XM_017009968.2:c.11143-2A>G
|
XP_016865457.1:n.11143-2A>G
|
|
|
XM_017009969.2:c.11143-2A>G
|
XP_016865458.1:n.11143-2A>G
|
|
|
XM_017009970.2:c.11143-2A>G
|
XP_016865459.1:n.11143-2A>G
|
|
|
XM_017009971.2:c.11143-2A>G
|
XP_016865460.1:n.11143-2A>G
|
|
|
XM_017009972.1:c.4261-2A>G
|
XP_016865461.1:n.4261-2A>G
|
|
|
XM_017009973.1:c.4240-2A>G
|
XP_016865462.1:n.4240-2A>G
|
|
|
NR_003149.2:n.11138-2A>G
|
|
|
