ENST00000357869.8:c.2079-77G>T
MANE Select
|
ENSP00000350536.4:n.2079-77G>T
|
|
ENST00000307885.4:c.2079-77G>T
|
ENSP00000311405.4:n.2079-77G>T
|
|
ENST00000357869.7:c.2079-77G>T
|
ENSP00000350536.3:n.2079-77G>T
|
|
ENST00000550422.5:c.2079-77G>T
|
ENSP00000446730.1:n.2079-77G>T
|
|
ENST00000552090.1:n.600+102G>T
|
|
|
NM_015270.3:c.2079-77G>T
|
NP_056085.1:n.2079-77G>T
|
|
NM_015270.4:c.2079-77G>T
|
NP_056085.1:n.2079-77G>T
|
|
NM_020983.2:c.2079-77G>T
|
NP_066193.1:n.2079-77G>T
|
|
XM_006719210.2:c.2079-77G>T
|
XP_006719273.1:n.2079-77G>T
|
|
XM_011537810.1:c.1980+448G>T
|
XP_011536112.1:n.1980+448G>T
|
|
XM_011537811.1:c.1980+448G>T
|
XP_011536113.1:n.1980+448G>T
|
|
XM_011537812.1:c.2079-77G>T
|
XP_011536114.1:n.2079-77G>T
|
|
XM_011537813.1:c.2079-77G>T
|
XP_011536115.1:n.2079-77G>T
|
|
XR_944483.1:n.2121-77G>T
|
|
|
XM_006719210.4:c.2079-77G>T
|
XP_006719273.1:n.2079-77G>T
|
|
XM_017018743.1:c.1980+448G>T
|
XP_016874232.1:n.1980+448G>T
|
|
XR_001748565.1:n.2079-77G>T
|
|
|
NM_015270.5:c.2079-77G>T
MANE Select
|
NP_056085.1:n.2079-77G>T
|
|
NM_001390830.1:c.2079-77G>T
|
NP_001377759.1:n.2079-77G>T
|
|
NM_001390831.1:c.2079-77G>T
|
NP_001377760.1:n.2079-77G>T
|
|