ENST00000330597.5:c.111A>G
(HBG1)
MANE Select
|
ENSP00000327431.4:p.Pro37=
|
|
ENST00000642908.1:c.316-1085A>G
|
ENSP00000495346.1:n.316-1085A>G
|
|
ENST00000647543.1:c.379-1085A>G
|
ENSP00000496470.1:n.379-1085A>G
|
|
ENST00000648735.1:n.162A>G
(HBG1)
|
|
|
ENST00000330597.3:c.111A>G
(HBG1)
|
ENSP00000327431.3:p.Pro37=
|
|
ENST00000620888.4:c.316-1085A>G
(HBG2)
|
ENSP00000479637.1:n.316-1085A>G
|
|
ENST00000623781.1:c.244T>C
|
ENSP00000485381.1:p.Trp82Arg
|
|
ENST00000632727.1:c.73A>G
(HBG1)
|
ENSP00000488759.1:p.Met25Val
|
|
NM_000559.2:c.111A>G
(HBG1)
|
NP_000550.2:p.Pro37=
|
|
NM_000559.3:c.111A>G
(HBG1)
MANE Select
|
NP_000550.2:p.Pro37=
|
|