|
NM_032119.4:c.12849+1G>T
MANE Select
|
NP_115495.3:n.12849+1G>T
|
|
ENST00000405460.9:c.12849+1G>T
MANE Select
|
ENSP00000384582.2:n.12849+1G>T
|
|
NM_032119.3:c.12849+1G>T
|
NP_115495.3:n.12849+1G>T
|
|
NR_003149.1:n.12862+1G>T
|
|
|
NR_003149.2:n.12865+1G>T
|
|
|
ENST00000405460.6:c.12849+1G>T
|
ENSP00000384582.2:n.12849+1G>T
|
|
ENST00000425867.3:c.1803+1G>T
|
ENSP00000392618.3:n.1803+1G>T
|
|
ENST00000639431.1:c.265+102401G>T
|
ENSP00000491057.1:n.265+102401G>T
|
|
ENST00000640464.1:n.3268+1G>T
|
|
|
XM_011543675.1:c.12846+1G>T
|
XP_011541977.1:n.12846+1G>T
|
|
XM_011543676.1:c.12768+1G>T
|
XP_011541978.1:n.12768+1G>T
|
|
XM_011543677.1:c.10152+1G>T
|
XP_011541979.1:n.10152+1G>T
|
|
XM_011543678.1:c.12849+1G>T
|
XP_011541980.1:n.12849+1G>T
|
|
XM_017009963.2:c.12870+1G>T
|
XP_016865452.1:n.12870+1G>T
|
|
XM_017009964.2:c.12867+1G>T
|
XP_016865453.1:n.12867+1G>T
|
|
XM_017009965.1:c.12867+1G>T
|
XP_016865454.1:n.12867+1G>T
|
|
XM_017009966.2:c.12789+1G>T
|
XP_016865455.1:n.12789+1G>T
|
|
XM_017009967.1:c.12774+1G>T
|
XP_016865456.1:n.12774+1G>T
|
|
XM_017009968.2:c.12870+1G>T
|
XP_016865457.1:n.12870+1G>T
|
|
XM_017009969.2:c.12870+1G>T
|
XP_016865458.1:n.12870+1G>T
|
|
XM_017009970.2:c.12870+1G>T
|
XP_016865459.1:n.12870+1G>T
|
|
XM_017009971.2:c.12870+1G>T
|
XP_016865460.1:n.12870+1G>T
|
|
XM_017009972.1:c.5988+1G>T
|
XP_016865461.1:n.5988+1G>T
|
|
XM_017009973.1:c.5967+1G>T
|
XP_016865462.1:n.5967+1G>T
|