ENST00000378043.9:c.-99A>G
MANE Select
|
ENSP00000367282.4:n.-99A>G
|
|
ENST00000378043.8:c.-99A>G
|
ENSP00000367282.4:n.-99A>G
|
|
ENST00000524877.5:n.6A>G
|
|
|
ENST00000524926.5:c.-99A>G
|
ENSP00000432681.1:n.-99A>G
|
|
ENST00000529265.5:n.13A>G
|
|
|
ENST00000533521.5:n.10A>G
|
|
|
ENST00000534553.5:c.-274A>G
|
ENSP00000431189.1:n.-274A>G
|
|
NM_001139443.1:c.-91A>G
|
NP_001132915.1:n.-91A>G
|
|
NM_001300786.1:c.-91A>G
|
NP_001287715.1:n.-91A>G
|
|
NM_001300787.1:c.-91A>G
|
NP_001287716.1:n.-91A>G
|
|
NM_004183.3:c.-99A>G
|
NP_004174.1:n.-99A>G
|
|
XM_005274210.2:c.-99A>G
|
XP_005274267.1:n.-99A>G
|
|
XM_005274216.2:c.-91A>G
|
XP_005274273.1:n.-91A>G
|
|
XM_005274218.3:c.-274A>G
|
XP_005274275.1:n.-274A>G
|
|
XM_005274219.2:c.-99A>G
|
XP_005274276.1:n.-99A>G
|
|
XM_005274221.2:c.-99A>G
|
XP_005274278.1:n.-99A>G
|
|
XM_011545229.1:c.-36-1406A>G
|
XP_011543531.1:n.-36-1406A>G
|
|
XM_011545230.1:c.59+3550A>G
|
XP_011543532.1:n.59+3550A>G
|
|
XM_011545231.1:c.-274A>G
|
XP_011543533.1:n.-274A>G
|
|
XM_011545232.1:c.-99A>G
|
XP_011543534.1:n.-99A>G
|
|
NM_001363592.1:c.-99A>G
|
NP_001350521.1:n.-99A>G
|
|
NR_134580.1:n.482A>G
|
|
|
XM_005274210.4:c.-99A>G
|
XP_005274267.1:n.-99A>G
|
|
XM_005274216.4:c.-91A>G
|
XP_005274273.1:n.-91A>G
|
|
XM_005274219.4:c.-99A>G
|
XP_005274276.1:n.-99A>G
|
|
XM_005274221.4:c.-99A>G
|
XP_005274278.1:n.-99A>G
|
|
XM_011545229.3:c.-36-1406A>G
|
XP_011543531.1:n.-36-1406A>G
|
|
XM_011545230.3:c.59+3550A>G
|
XP_011543532.1:n.59+3550A>G
|
|
XR_001747952.2:n.588A>G
|
|
|
XR_001747953.2:n.592A>G
|
|
|
XR_001747954.2:n.592A>G
|
|
|
NM_004183.4:c.-99A>G
MANE Select
|
NP_004174.1:n.-99A>G
|
|
NM_001139443.2:c.-91A>G
|
NP_001132915.1:n.-91A>G
|
|
NM_001300786.2:c.-91A>G
|
NP_001287715.1:n.-91A>G
|
|
NM_001300787.2:c.-91A>G
|
NP_001287716.1:n.-91A>G
|
|
NR_134580.2:n.15A>G
|
|
|