ENST00000273951.13:c.*34T>G
MANE Select
|
ENSP00000273951.8:n.*34T>G
|
|
ENST00000273951.12:c.*34T>G
|
ENSP00000273951.8:n.*34T>G
|
|
ENST00000503364.5:n.132T>G
|
|
|
ENST00000503472.5:n.1343T>G
|
|
|
ENST00000504199.5:c.*34T>G
|
ENSP00000421725.1:n.*34T>G
|
|
ENST00000509740.5:c.*282T>G
|
ENSP00000422664.1:n.*282T>G
|
|
ENST00000513476.5:c.1404T>G
|
ENSP00000426683.1:p.Val468=
|
|
NM_000583.3:c.*34T>G
|
NP_000574.2:n.*34T>G
|
|
NM_001204306.1:c.*34T>G
|
NP_001191235.1:n.*34T>G
|
|
NM_001204307.1:c.*34T>G
|
NP_001191236.1:n.*34T>G
|
|
XM_006714177.2:c.*48T>G
|
XP_006714240.1:n.*48T>G
|
|
XM_006714177.3:c.*48T>G
|
XP_006714240.1:n.*48T>G
|
|
NM_000583.4:c.*34T>G
MANE Select
|
NP_000574.2:n.*34T>G
|
|