ENST00000273951.13:c.1301C>G
MANE Select
|
ENSP00000273951.8:p.Thr434Arg
|
|
ENST00000273951.12:c.1301C>G
|
ENSP00000273951.8:p.Thr434Arg
|
|
ENST00000503364.5:n.68+1799C>G
|
|
|
ENST00000503472.5:n.1185C>G
|
|
|
ENST00000504199.5:c.1358C>G
|
ENSP00000421725.1:p.Thr453Arg
|
|
ENST00000509740.5:c.*124C>G
|
ENSP00000422664.1:n.*124C>G
|
|
ENST00000513476.5:c.1301C>G
|
ENSP00000426683.1:p.Thr434Arg
|
|
NM_000583.3:c.1301C>G
|
NP_000574.2:p.Thr434Arg
|
|
NM_001204306.1:c.1301C>G
|
NP_001191235.1:p.Thr434Arg
|
|
NM_001204307.1:c.1358C>G
|
NP_001191236.1:p.Thr453Arg
|
|
XM_006714177.2:c.1262+1799C>G
|
XP_006714240.1:n.1262+1799C>G
|
|
XM_006714177.3:c.1262+1799C>G
|
XP_006714240.1:n.1262+1799C>G
|
|
NM_000583.4:c.1301C>G
MANE Select
|
NP_000574.2:p.Thr434Arg
|
|