|
NM_032119.4:c.12850-1G>T
MANE Select
|
NP_115495.3:n.12850-1G>T
|
|
ENST00000405460.9:c.12850-1G>T
MANE Select
|
ENSP00000384582.2:n.12850-1G>T
|
|
NM_032119.3:c.12850-1G>T
|
NP_115495.3:n.12850-1G>T
|
|
NR_003149.1:n.12863-1G>T
|
|
|
NR_003149.2:n.12866-1G>T
|
|
|
ENST00000405460.6:c.12850-1G>T
|
ENSP00000384582.2:n.12850-1G>T
|
|
ENST00000425867.3:c.1804-1G>T
|
ENSP00000392618.3:n.1804-1G>T
|
|
ENST00000639431.1:c.265+102655G>T
|
ENSP00000491057.1:n.265+102655G>T
|
|
ENST00000640464.1:n.3269-1G>T
|
|
|
XM_011543675.1:c.12847-1G>T
|
XP_011541977.1:n.12847-1G>T
|
|
XM_011543676.1:c.12769-1G>T
|
XP_011541978.1:n.12769-1G>T
|
|
XM_011543677.1:c.10153-1G>T
|
XP_011541979.1:n.10153-1G>T
|
|
XM_011543678.1:c.12850-1G>T
|
XP_011541980.1:n.12850-1G>T
|
|
XM_017009963.2:c.12871-1G>T
|
XP_016865452.1:n.12871-1G>T
|
|
XM_017009964.2:c.12868-1G>T
|
XP_016865453.1:n.12868-1G>T
|
|
XM_017009965.1:c.12868-1G>T
|
XP_016865454.1:n.12868-1G>T
|
|
XM_017009966.2:c.12790-1G>T
|
XP_016865455.1:n.12790-1G>T
|
|
XM_017009967.1:c.12775-1G>T
|
XP_016865456.1:n.12775-1G>T
|
|
XM_017009968.2:c.12871-1G>T
|
XP_016865457.1:n.12871-1G>T
|
|
XM_017009969.2:c.12871-1G>T
|
XP_016865458.1:n.12871-1G>T
|
|
XM_017009970.2:c.12871-1G>T
|
XP_016865459.1:n.12871-1G>T
|
|
XM_017009971.2:c.12871-1G>T
|
XP_016865460.1:n.12871-1G>T
|
|
XM_017009972.1:c.5989-1G>T
|
XP_016865461.1:n.5989-1G>T
|
|
XM_017009973.1:c.5968-1G>T
|
XP_016865462.1:n.5968-1G>T
|