ENST00000424685.3:c.2392C=
|
ENSP00000388446.3:p.His798=
|
|
ENST00000428762.6:c.2392C=
MANE Select
|
ENSP00000392423.1:p.His798=
|
|
ENST00000473457.2:n.2656C=
|
|
|
ENST00000679867.1:n.2276C=
|
|
|
ENST00000680706.1:n.95C=
|
|
|
ENST00000680712.1:n.2109C=
|
|
|
ENST00000681034.1:c.2392C=
|
ENSP00000506075.1:p.His798=
|
|
ENST00000343529.9:c.2392C=
|
ENSP00000345694.5:p.His798=
|
|
ENST00000424685.2:c.2392C=
|
ENSP00000388446.2:p.His798=
|
|
ENST00000428762.5:c.2392C=
|
ENSP00000392423.1:p.His798=
|
|
NM_005045.3:c.2392C=
|
NP_005036.2:p.His798=
|
|
NM_173054.2:c.2392C=
|
NP_774959.1:p.His798=
|
|
NM_005045.4:c.2392C=
MANE Select
|
NP_005036.2:p.His798=
|
|
NM_173054.3:c.2392C=
|
NP_774959.1:p.His798=
|
|