ENST00000273951.13:c.*47G>T
MANE Select
|
ENSP00000273951.8:n.*47G>T
|
|
ENST00000273951.12:c.*47G>T
|
ENSP00000273951.8:n.*47G>T
|
|
ENST00000503364.5:n.145G>T
|
|
|
ENST00000503472.5:n.1356G>T
|
|
|
ENST00000504199.5:c.*47G>T
|
ENSP00000421725.1:n.*47G>T
|
|
ENST00000509740.5:c.*295G>T
|
ENSP00000422664.1:n.*295G>T
|
|
ENST00000513476.5:c.1417G>T
|
ENSP00000426683.1:p.Gly473Trp
|
|
NM_000583.3:c.*47G>T
|
NP_000574.2:n.*47G>T
|
|
NM_001204306.1:c.*47G>T
|
NP_001191235.1:n.*47G>T
|
|
NM_001204307.1:c.*47G>T
|
NP_001191236.1:n.*47G>T
|
|
XM_006714177.2:c.*61G>T
|
XP_006714240.1:n.*61G>T
|
|
XM_006714177.3:c.*61G>T
|
XP_006714240.1:n.*61G>T
|
|
NM_000583.4:c.*47G>T
MANE Select
|
NP_000574.2:n.*47G>T
|
|