ENST00000304494.10:c.*9G>T
MANE Select
|
ENSP00000307101.5:n.*9G>T
|
|
ENST00000404796.3:c.348-61213C>A
|
ENSP00000385916.2:n.348-61213C>A
|
|
ENST00000579755.2:c.*124G>T
MANE Plus Clinical
|
ENSP00000462950.1:n.*124G>T
|
|
ENST00000304494.9:c.*9G>T
|
ENSP00000307101.5:n.*9G>T
|
|
ENST00000361570.4:c.*9G>T
|
ENSP00000355153.4:n.*9G>T
|
|
ENST00000380151.3:c.754G>T
|
ENSP00000369496.3:n.754G>T
|
|
ENST00000404796.2:c.348-61213C>A
|
ENSP00000385916.2:n.348-61213C>A
|
|
ENST00000494262.5:c.*9G>T
|
ENSP00000464952.1:n.*9G>T
|
|
ENST00000498124.1:c.*173G>T
|
ENSP00000418915.1:n.*173G>T
|
|
ENST00000498628.6:c.*9G>T
|
ENSP00000467857.1:n.*9G>T
|
|
ENST00000530628.2:c.*50G>T
|
ENSP00000432664.2:n.*50G>T
|
|
ENST00000578845.2:c.*9G>T
|
ENSP00000467390.1:n.*9G>T
|
|
ENST00000579122.1:c.406G>T
|
ENSP00000464202.1:p.Glu136Ter
|
|
ENST00000579755.1:c.*124G>T
|
ENSP00000462950.1:n.*124G>T
|
|
NM_000077.4:c.*9G>T , LRG_11t1:c.*9G>T
|
NP_000068.1:n.*9G>T
|
|
NM_001195132.1:c.*173G>T
|
NP_001182061.1:n.*173G>T
|
|
NM_058195.3:c.*124G>T , LRG_11t2:c.*124G>T
|
NP_478102.2:n.*124G>T
|
|
NM_058197.4:c.754G>T
|
NP_478104.2:n.754G>T
|
|
XM_005251343.1:c.*9G>T
|
XP_005251400.1:n.*9G>T
|
|
XM_011517679.1:c.*9G>T
|
XP_011515981.1:n.*9G>T
|
|
NM_001363763.1:c.*9G>T
|
NP_001350692.1:n.*9G>T
|
|
NM_001363763.2:c.*9G>T
|
NP_001350692.1:n.*9G>T
|
|
NM_000077.5:c.*9G>T
MANE Select
|
NP_000068.1:n.*9G>T
|
|
NM_001195132.2:c.*173G>T
|
NP_001182061.1:n.*173G>T
|
|
NM_058195.4:c.*124G>T
MANE Plus Clinical
|
NP_478102.2:n.*124G>T
|
|
NM_058197.5:c.*403G>T
|
NP_478104.2:n.*403G>T
|
|