ENST00000405460.9:c.16368+149C>G
MANE Select
|
ENSP00000384582.2:n.16368+149C>G
|
|
ENST00000425867.3:c.5322+149C>G
|
ENSP00000392618.3:n.5322+149C>G
|
|
ENST00000638510.1:n.3635+149C>G
|
|
|
ENST00000639431.1:c.265+147536C>G
|
ENSP00000491057.1:n.265+147536C>G
|
|
ENST00000640061.1:n.128+1563C>G
|
|
|
ENST00000640407.1:c.2778+149C>G
|
ENSP00000491425.1:n.2778+149C>G
|
|
ENST00000405460.6:c.16368+149C>G
|
ENSP00000384582.2:n.16368+149C>G
|
|
ENST00000425867.2:c.3351+149C>G
|
ENSP00000392618.2:n.3351+149C>G
|
|
NM_032119.3:c.16368+149C>G
|
NP_115495.3:n.16368+149C>G
|
|
NR_003149.1:n.16381+149C>G
|
|
|
XM_011543675.1:c.16365+149C>G
|
XP_011541977.1:n.16365+149C>G
|
|
XM_011543676.1:c.16287+149C>G
|
XP_011541978.1:n.16287+149C>G
|
|
XM_011543677.1:c.13671+149C>G
|
XP_011541979.1:n.13671+149C>G
|
|
NM_032119.4:c.16368+149C>G
MANE Select
|
NP_115495.3:n.16368+149C>G
|
|
XM_017009963.2:c.16389+149C>G
|
XP_016865452.1:n.16389+149C>G
|
|
XM_017009964.2:c.16386+149C>G
|
XP_016865453.1:n.16386+149C>G
|
|
XM_017009965.1:c.16386+149C>G
|
XP_016865454.1:n.16386+149C>G
|
|
XM_017009966.2:c.16308+149C>G
|
XP_016865455.1:n.16308+149C>G
|
|
XM_017009967.1:c.16293+149C>G
|
XP_016865456.1:n.16293+149C>G
|
|
XM_017009968.2:c.16209+149C>G
|
XP_016865457.1:n.16209+149C>G
|
|
XM_017009969.2:c.16389+149C>G
|
XP_016865458.1:n.16389+149C>G
|
|
XM_017009972.1:c.9507+149C>G
|
XP_016865461.1:n.9507+149C>G
|
|
XM_017009973.1:c.9486+149C>G
|
XP_016865462.1:n.9486+149C>G
|
|
NR_003149.2:n.16384+149C>G
|
|
|