ENST00000478003.2:n.1865-11C>A
|
|
|
ENST00000682276.1:n.1482-11C>A
|
|
|
ENST00000682892.1:c.1584-11C>A
|
ENSP00000507214.1:n.1584-11C>A
|
|
ENST00000682952.1:n.1676-11C>A
|
|
|
ENST00000684455.1:c.1250-11C>A
|
|
|
ENST00000684642.1:c.1434-11C>A
|
ENSP00000507355.1:n.1434-11C>A
|
|
ENST00000684740.1:n.2215-11C>A
|
|
|
ENST00000303236.9:c.2037-11C>A
MANE Select
|
ENSP00000307235.3:n.2037-11C>A
|
|
ENST00000652099.1:c.2231-11C>A
|
|
|
ENST00000652736.1:n.1913-11C>A
|
|
|
ENST00000303236.7:c.2037-11C>A
|
ENSP00000307235.3:n.2037-11C>A
|
|
ENST00000415570.1:c.1674-11C>A
|
ENSP00000412076.1:n.1674-11C>A
|
|
ENST00000419748.5:c.1584-11C>A
|
ENSP00000408325.1:n.1584-11C>A
|
|
ENST00000478003.1:n.603-11C>A
|
|
|
NM_001313915.1:c.1584-11C>A
|
NP_001300844.1:n.1584-11C>A
|
|
NM_004836.5:c.2037-11C>A
|
NP_004827.4:n.2037-11C>A
|
|
NM_004836.6:c.2037-11C>A
|
NP_004827.4:n.2037-11C>A
|
|
NR_110236.1:n.1594G>T
|
|
|
XM_005264649.3:c.1353-11C>A
|
XP_005264706.1:n.1353-11C>A
|
|
XR_939749.1:n.2316-11C>A
|
|
|
XM_017005376.2:c.1353-11C>A
|
XP_016860865.1:n.1353-11C>A
|
|
NM_004836.7:c.2037-11C>A
MANE Select
|
NP_004827.4:n.2037-11C>A
|
|
NM_001313915.2:c.1584-11C>A
|
NP_001300844.1:n.1584-11C>A
|
|