ENST00000330597.5:c.138T=
(HBG1)
MANE Select
|
ENSP00000327431.4:p.Phe46=
|
|
ENST00000642908.1:c.316-1058T=
|
ENSP00000495346.1:n.316-1058T=
|
|
ENST00000647543.1:c.379-1058T=
|
ENSP00000496470.1:n.379-1058T=
|
|
ENST00000648735.1:n.189T=
(HBG1)
|
|
|
ENST00000330597.3:c.138T=
(HBG1)
|
ENSP00000327431.3:p.Phe46=
|
|
ENST00000620888.4:c.316-1058T=
(HBG2)
|
ENSP00000479637.1:n.316-1058T=
|
|
ENST00000623781.1:c.217A=
|
ENSP00000485381.1:p.Lys73=
|
|
ENST00000632727.1:c.*7T=
(HBG1)
|
ENSP00000488759.1:n.*7T=
|
|
NM_000559.2:c.138T=
(HBG1)
|
NP_000550.2:p.Phe46=
|
|
NM_000559.3:c.138T=
(HBG1)
MANE Select
|
NP_000550.2:p.Phe46=
|
|