ENST00000699947.1:c.2313G=
|
ENSP00000514703.1:p.Val771=
|
|
ENST00000699948.1:c.*626G=
|
ENSP00000514704.1:n.*626G=
|
|
ENST00000382745.9:c.2313G=
MANE Select
|
ENSP00000372193.4:p.Val771=
|
|
ENST00000262318.12:c.2242G=
|
ENSP00000262318.8:p.Gly748=
|
|
ENST00000382745.8:c.2313G=
|
ENSP00000372193.4:p.Val771=
|
|
ENST00000448525.5:c.2241G=
|
ENSP00000410907.1:p.Val747=
|
|
ENST00000563642.6:n.2382G=
|
|
|
ENST00000565092.6:n.1348G=
|
|
|
ENST00000567836.2:n.554G=
|
|
|
NM_001114331.2:c.2241G=
|
NP_001107803.1:p.Val747=
|
|
NM_001287.5:c.2313G=
|
NP_001278.1:p.Val771=
|
|
XM_011522354.1:c.2139G=
|
XP_011520656.1:p.Val713=
|
|
NM_001287.6:c.2313G=
MANE Select
|
NP_001278.1:p.Val771=
|
|
NM_001114331.3:c.2241G=
|
NP_001107803.1:p.Val747=
|
|