ENST00000697337.1:c.*2578G=
|
ENSP00000513259.1:n.*2578G=
|
|
ENST00000697338.1:c.1690G=
|
ENSP00000513260.1:n.1690G=
|
|
ENST00000697339.1:c.876G=
|
ENSP00000513261.1:p.Glu292=
|
|
ENST00000697340.1:c.*559G=
|
ENSP00000513262.1:n.*559G=
|
|
ENST00000697341.1:n.1812G=
|
|
|
ENST00000313735.11:c.1842G=
MANE Select
|
ENSP00000327251.6:p.Glu614=
|
|
ENST00000646938.1:c.1839G=
|
ENSP00000494870.1:p.Glu613=
|
|
ENST00000313735.10:c.1842G=
|
ENSP00000327251.6:p.Glu614=
|
|
ENST00000621962.1:c.1725G=
|
ENSP00000482291.1:p.Glu575=
|
|
NM_000625.4:c.1842G=
MANE Select
|
NP_000616.3:p.Glu614=
|
|
XM_011524859.1:c.1842G=
|
XP_011523161.1:p.Glu614=
|
|
XM_011524860.1:c.1839G=
|
XP_011523162.1:p.Glu613=
|
|
XM_011524861.1:c.1842G=
|
XP_011523163.1:p.Glu614=
|
|
XM_011524862.1:c.1176G=
|
XP_011523164.1:p.Glu392=
|
|