ENST00000433363.7:c.919C>A
MANE Select
|
ENSP00000406220.2:p.Arg307=
|
|
ENST00000293800.10:c.868C>A
|
ENSP00000293800.6:p.Arg290=
|
|
ENST00000381074.8:c.790C>A
|
ENSP00000370464.4:p.Arg264=
|
|
ENST00000433363.6:c.919C>A
|
ENSP00000406220.2:p.Arg307=
|
|
ENST00000572094.1:c.*669C>A
|
ENSP00000461495.1:n.*669C>A
|
|
ENST00000572727.1:n.28C>A
|
|
|
ENST00000573648.5:c.919C>A
|
ENSP00000459372.1:p.Arg307=
|
|
ENST00000574824.5:n.2052C>A
|
|
|
NM_001143838.2:c.919C>A
|
NP_001137310.1:p.Arg307=
|
|
NM_001284509.1:c.868C>A
|
NP_001271438.1:p.Arg290=
|
|
NM_001284510.1:c.790C>A
|
NP_001271439.1:p.Arg264=
|
|
NM_177550.4:c.919C>A , LRG_1020t1:c.919C>A
|
NP_808218.1:p.Arg307=
|
|
XM_006721504.2:c.808C>A
|
XP_006721567.1:p.Arg270=
|
|
XM_011523795.1:c.919C>A
|
XP_011522097.1:p.Arg307=
|
|
XM_011523795.3:c.919C>A
|
XP_011522097.1:p.Arg307=
|
|
NM_001143838.3:c.919C>A
|
NP_001137310.1:p.Arg307=
|
|
NM_001284509.2:c.868C>A
|
NP_001271438.1:p.Arg290=
|
|
NM_001284510.2:c.790C>A
|
NP_001271439.1:p.Arg264=
|
|
NM_177550.5:c.919C>A
MANE Select
|
NP_808218.1:p.Arg307=
|
|