ENST00000354105.10:c.1143G=
MANE Select
|
ENSP00000326411.6:p.Val381=
|
|
ENST00000354105.8:c.1143G=
|
ENSP00000326411.6:p.Val381=
|
|
ENST00000370379.1:c.408G=
|
ENSP00000359405.1:p.Val136=
|
|
ENST00000468709.5:n.999G=
|
|
|
ENST00000478047.1:n.1298G=
|
|
|
ENST00000482452.5:n.826G=
|
|
|
NM_001303404.1:c.1143G=
|
NP_001290333.1:p.Val381=
|
|
NM_001303405.1:c.732G=
|
NP_001290334.1:p.Val244=
|
|
NM_001303406.1:c.732G=
|
NP_001290335.1:p.Val244=
|
|
NM_001303407.1:c.408G=
|
NP_001290336.1:p.Val136=
|
|
NM_018294.5:c.1143G=
|
NP_060764.3:p.Val381=
|
|
NM_018294.6:c.1143G=
MANE Select
|
NP_060764.3:p.Val381=
|
|
NM_001303404.2:c.1143G=
|
NP_001290333.1:p.Val381=
|
|
NM_001303405.2:c.732G=
|
NP_001290334.1:p.Val244=
|
|
NM_001303406.2:c.732G=
|
NP_001290335.1:p.Val244=
|
|
NM_001303407.2:c.408G=
|
NP_001290336.1:p.Val136=
|
|