ENST00000330597.5:c.46_57dup
(HBG1)
MANE Select
|
ENSP00000327431.4:p.Val19_Asn20insTrpGlyLysVal
|
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ENST00000642908.1:c.316-1272_316-1261dup
|
ENSP00000495346.1:n.316-1272_316-1261dup
|
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ENST00000647543.1:c.379-1272_379-1261dup
|
ENSP00000496470.1:n.379-1272_379-1261dup
|
|
ENST00000648735.1:n.97_108dup
(HBG1)
|
|
|
ENST00000330597.3:c.46_57dup
(HBG1)
|
ENSP00000327431.3:p.Val19_Asn20insTrpGlyLysVal
|
|
ENST00000620888.4:c.316-1272_316-1261dup
(HBG2)
|
ENSP00000479637.1:n.316-1272_316-1261dup
|
|
ENST00000623781.1:c.303_314dup
|
ENSP00000485381.1:p.Pro104_Gln105insHisLeuAlaPro
|
|
ENST00000632727.1:c.46_54+3dup
(HBG1)
|
|
|
NM_000559.2:c.46_57dup
(HBG1)
|
NP_000550.2:p.Val19_Asn20insTrpGlyLysVal
|
|
NM_000559.3:c.46_57dup
(HBG1)
MANE Select
|
NP_000550.2:p.Val19_Asn20insTrpGlyLysVal
|
|