ENST00000436193.6:c.-131G>T
|
ENSP00000394277.2:n.-131G>T
|
|
ENST00000671928.2:c.-17+302G>T
|
ENSP00000500069.2:n.-17+302G>T
|
|
ENST00000672892.2:c.-17+302G>T
|
ENSP00000499944.2:n.-17+302G>T
|
|
ENST00000303498.10:c.-293+302G>T
|
ENSP00000306477.6:n.-293+302G>T
|
|
ENST00000417015.3:c.-17+302G>T
|
ENSP00000403775.3:n.-17+302G>T
|
|
ENST00000427382.2:c.-17+549G>T
|
ENSP00000397113.2:n.-17+549G>T
|
|
ENST00000437172.6:c.-205+302G>T
|
ENSP00000400995.2:n.-205+302G>T
|
|
ENST00000449107.7:c.-17+426G>T
|
ENSP00000388212.2:n.-17+426G>T
|
|
ENST00000467027.6:n.433G>T
|
|
|
ENST00000642517.1:n.59G>T
|
|
|
ENST00000643237.3:c.-17+302G>T
MANE Select
|
ENSP00000495254.2:n.-17+302G>T
|
|
ENST00000646371.1:c.-293+426G>T
|
ENSP00000495866.1:n.-293+426G>T
|
|
ENST00000672065.1:c.44+302G>T
|
ENSP00000500403.1:n.44+302G>T
|
|
ENST00000672112.1:c.-139+302G>T
|
ENSP00000500193.1:n.-139+302G>T
|
|
ENST00000672141.1:c.-17+302G>T
|
ENSP00000500210.1:n.-17+302G>T
|
|
ENST00000672336.1:c.-407G>T
|
ENSP00000500267.1:n.-407G>T
|
|
ENST00000672427.1:c.-17+302G>T
|
ENSP00000500131.1:n.-17+302G>T
|
|
ENST00000672760.1:c.-17+302G>T
|
ENSP00000500530.1:n.-17+302G>T
|
|
ENST00000672968.1:n.20+426G>T
|
|
|
ENST00000673467.1:c.-17+302G>T
|
ENSP00000500288.1:n.-17+302G>T
|
|
ENST00000673620.1:c.-17+426G>T
|
ENSP00000500325.1:n.-17+426G>T
|
|
ENST00000303498.9:c.44+302G>T
|
ENSP00000306477.5:n.44+302G>T
|
|
ENST00000383778.5:c.-131G>T
|
ENSP00000373288.4:n.-131G>T
|
|
ENST00000417015.1:c.*295+302G>T
|
ENSP00000403775.1:n.*295+302G>T
|
|
ENST00000427382.1:c.-17+549G>T
|
ENSP00000397113.1:n.-17+549G>T
|
|
ENST00000436193.5:c.-131G>T
|
ENSP00000394277.1:n.-131G>T
|
|
ENST00000437172.5:c.-139+302G>T
|
ENSP00000400995.1:n.-139+302G>T
|
|
ENST00000449107.5:c.50+426G>T
|
ENSP00000388212.1:n.50+426G>T
|
|
ENST00000467027.5:n.94+302G>T
|
|
|
ENST00000471964.5:n.184G>T
|
|
|
ENST00000480711.1:n.147+302G>T
|
|
|
ENST00000494021.1:n.401+426G>T
|
|
|
NM_000060.3:c.44+302G>T
|
NP_000051.1:n.44+302G>T
|
|
NM_001281723.1:c.50+426G>T
|
NP_001268652.1:n.50+426G>T
|
|
NM_001281724.1:c.-139+302G>T
|
NP_001268653.1:n.-139+302G>T
|
|
NM_001281725.1:c.-131G>T
|
NP_001268654.1:n.-131G>T
|
|
NM_001281726.1:c.44+302G>T
|
NP_001268655.1:n.44+302G>T
|
|
XM_006713314.2:c.-293+302G>T
|
XP_006713377.1:n.-293+302G>T
|
|
XM_011534041.1:c.-131G>T
|
XP_011532343.1:n.-131G>T
|
|
NM_000060.4:c.44+302G>T
|
NP_000051.1:n.44+302G>T
|
|
NM_001281723.2:c.50+426G>T
|
NP_001268652.1:n.50+426G>T
|
|
NM_001281724.2:c.-139+302G>T
|
NP_001268653.1:n.-139+302G>T
|
|
NM_001281725.2:c.-131G>T
|
NP_001268654.1:n.-131G>T
|
|
NM_001323582.1:c.-293+302G>T
|
NP_001310511.1:n.-293+302G>T
|
|
XM_011534041.2:c.-131G>T
|
XP_011532343.1:n.-131G>T
|
|
XM_017007088.1:c.-407G>T
|
XP_016862577.1:n.-407G>T
|
|
NM_001281723.3:c.-17+426G>T
|
NP_001268652.2:n.-17+426G>T
|
|
NM_001281724.3:c.-205+302G>T
|
NP_001268653.2:n.-205+302G>T
|
|
NM_001370658.1:c.-17+302G>T
MANE Select
|
NP_001357587.1:n.-17+302G>T
|
|
NM_001370752.1:c.-17+302G>T
|
NP_001357681.1:n.-17+302G>T
|
|
NM_001370753.1:c.-17+302G>T
|
NP_001357682.1:n.-17+302G>T
|
|
NM_001281726.2:c.-17+302G>T
|
NP_001268655.2:n.-17+302G>T
|
|