ENST00000261192.12:c.1119+1110T>A
MANE Select
|
ENSP00000261192.7:n.1119+1110T>A
|
|
ENST00000261192.11:c.1119+1110T>A
|
ENSP00000261192.7:n.1119+1110T>A
|
|
ENST00000342945.9:c.936+1110T>A
|
ENSP00000339805.5:n.936+1110T>A
|
|
ENST00000538118.5:c.1116+1110T>A
|
ENSP00000440817.1:n.1116+1110T>A
|
|
ENST00000539282.5:c.1155+1110T>A
|
ENSP00000443459.1:n.1155+1110T>A
|
|
ENST00000539780.5:c.1008+1110T>A
|
ENSP00000440827.1:n.1008+1110T>A
|
|
ENST00000543099.1:n.174+1110T>A
|
|
|
NM_001178091.1:c.1008+1110T>A
|
NP_001171562.1:n.1008+1110T>A
|
|
NM_001178092.1:c.936+1110T>A
|
NP_001171563.1:n.936+1110T>A
|
|
NM_001178093.1:c.1155+1110T>A
|
NP_001171564.1:n.1155+1110T>A
|
|
NM_001178094.1:c.1116+1110T>A
|
NP_001171565.1:n.1116+1110T>A
|
|
NM_005504.6:c.1119+1110T>A
|
NP_005495.2:n.1119+1110T>A
|
|
XM_011520810.1:c.1155+1110T>A
|
XP_011519112.1:n.1155+1110T>A
|
|
XR_931441.1:n.1532-1988A>T
|
|
|
XR_931442.1:n.1532-1988A>T
|
|
|
XR_931443.1:n.1439-1988A>T
|
|
|
XM_017019768.2:c.1221+1110T>A
|
XP_016875257.1:n.1221+1110T>A
|
|
XR_001748835.2:n.4171+1110T>A
|
|
|
XR_001749047.1:n.3978-1988A>T
|
|
|
XR_001749048.2:n.3978-1988A>T
|
|
|
XR_001749049.1:n.3885-1988A>T
|
|
|
NM_005504.7:c.1119+1110T>A
MANE Select
|
NP_005495.2:n.1119+1110T>A
|
|
NM_001178091.2:c.1008+1110T>A
|
NP_001171562.1:n.1008+1110T>A
|
|
NM_001178092.2:c.936+1110T>A
|
NP_001171563.1:n.936+1110T>A
|
|
NM_001178093.2:c.1155+1110T>A
|
NP_001171564.1:n.1155+1110T>A
|
|
NM_001178094.2:c.1116+1110T>A
|
NP_001171565.1:n.1116+1110T>A
|
|