ENST00000330597.5:c.292_295dup
(HBG1)
MANE Select
|
ENSP00000327431.4:p.Val99AlafsTer5
|
|
ENST00000642908.1:c.316-904_316-901dup
|
ENSP00000495346.1:n.316-904_316-901dup
|
|
ENST00000647543.1:c.379-904_379-901dup
|
ENSP00000496470.1:n.379-904_379-901dup
|
|
ENST00000648735.1:n.343_346dup
(HBG1)
|
|
|
ENST00000330597.3:c.292_295dup
(HBG1)
|
ENSP00000327431.3:p.Val99AlafsTer5
|
|
ENST00000620888.4:c.316-904_316-901dup
(HBG2)
|
ENSP00000479637.1:n.316-904_316-901dup
|
|
ENST00000623781.1:c.62_65dup
|
ENSP00000485381.1:p.Gln22HisfsTer17
|
|
ENST00000632727.1:c.*161_*164dup
(HBG1)
|
ENSP00000488759.1:n.*161_*164dup
|
|
NM_000559.2:c.292_295dup
(HBG1)
|
NP_000550.2:p.Val99AlafsTer5
|
|
NM_000559.3:c.292_295dup
(HBG1)
MANE Select
|
NP_000550.2:p.Val99AlafsTer5
|
|