ENST00000330597.5:c.121A>C
(HBG1)
MANE Select
|
ENSP00000327431.4:p.Arg41=
|
|
ENST00000642908.1:c.316-1075A>C
|
ENSP00000495346.1:n.316-1075A>C
|
|
ENST00000647543.1:c.379-1075A>C
|
ENSP00000496470.1:n.379-1075A>C
|
|
ENST00000648735.1:n.172A>C
(HBG1)
|
|
|
ENST00000330597.3:c.121A>C
(HBG1)
|
ENSP00000327431.3:p.Arg41=
|
|
ENST00000620888.4:c.316-1075A>C
(HBG2)
|
ENSP00000479637.1:n.316-1075A>C
|
|
ENST00000623781.1:c.234T>G
|
ENSP00000485381.1:p.Pro78=
|
|
ENST00000632727.1:c.83A>C
(HBG1)
|
ENSP00000488759.1:p.Glu28Ala
|
|
NM_000559.2:c.121A>C
(HBG1)
|
NP_000550.2:p.Arg41=
|
|
NM_000559.3:c.121A>C
(HBG1)
MANE Select
|
NP_000550.2:p.Arg41=
|
|