|
ENST00000299882.11:c.663G>T
MANE Select
|
ENSP00000299882.5:p.Gly221=
|
|
|
ENST00000545579.6:c.636G>T
|
ENSP00000441104.1:p.Gly212=
|
|
|
ENST00000645981.1:c.*632G>T
|
ENSP00000496410.1:n.*632G>T
|
|
|
ENST00000299882.9:c.663G>T
|
ENSP00000299882.5:p.Gly221=
|
|
|
ENST00000536856.5:c.-115G>T
|
ENSP00000437937.1:n.-115G>T
|
|
|
ENST00000538770.1:c.-115G>T
|
ENSP00000445502.1:n.-115G>T
|
|
|
ENST00000538955.5:c.531G>T
|
ENSP00000445528.1:p.Gly177=
|
|
|
ENST00000539732.5:c.-115G>T
|
ENSP00000443681.1:n.-115G>T
|
|
|
ENST00000540540.5:c.-115G>T
|
ENSP00000437761.1:n.-115G>T
|
|
|
ENST00000544476.1:c.447-1351G>T
|
ENSP00000445930.1:n.447-1351G>T
|
|
|
ENST00000544634.5:c.579-1351G>T
|
ENSP00000440783.1:n.579-1351G>T
|
|
|
ENST00000545579.5:c.636G>T
|
ENSP00000441104.1:p.Gly212=
|
|
|
NM_001288749.1:c.447-1351G>T
|
NP_001275678.1:n.447-1351G>T
|
|
|
NM_001288750.1:c.531G>T
|
NP_001275679.1:p.Gly177=
|
|
|
NM_001288751.1:c.636G>T
|
NP_001275680.1:p.Gly212=
|
|
|
NM_001288752.1:c.579-1351G>T
|
NP_001275681.1:n.579-1351G>T
|
|
|
NM_030770.3:c.663G>T
|
NP_110397.2:p.Gly221=
|
|
|
NR_110046.1:n.610G>T
|
|
|
|
NR_110047.1:n.610G>T
|
|
|
|
XM_011543014.1:c.654G>T
|
XP_011541316.1:p.Gly218=
|
|
|
XM_011543015.1:c.663G>T
|
XP_011541317.1:p.Gly221=
|
|
|
XM_011543016.1:c.663G>T
|
XP_011541318.1:p.Gly221=
|
|
|
XM_017018366.1:c.-1256G>T
|
XP_016873855.1:n.-1256G>T
|
|
|
XM_017018367.1:c.-1256G>T
|
XP_016873856.1:n.-1256G>T
|
|
|
XR_001747990.1:n.4250G>T
|
|
|
|
XR_001747991.1:n.4354G>T
|
|
|
|
XR_001747992.1:n.4147G>T
|
|
|
|
NM_030770.4:c.663G>T
MANE Select
|
NP_110397.2:p.Gly221=
|
|
|
NM_001288749.2:c.447-1351G>T
|
NP_001275678.1:n.447-1351G>T
|
|
|
NM_001288750.2:c.531G>T
|
NP_001275679.1:p.Gly177=
|
|
|
NM_001288752.2:c.579-1351G>T
|
NP_001275681.1:n.579-1351G>T
|
|
|
NR_110046.2:n.545G>T
|
|
|
|
NR_110047.2:n.545G>T
|
|
|
|
NM_001288751.2:c.636G>T
|
NP_001275680.1:p.Gly212=
|
|
