ENST00000354105.10:c.936T=
MANE Select
|
ENSP00000326411.6:p.Ser312=
|
|
ENST00000354105.8:c.936T=
|
ENSP00000326411.6:p.Ser312=
|
|
ENST00000370379.1:c.201T=
|
ENSP00000359405.1:p.Ser67=
|
|
ENST00000466408.1:n.290T=
|
|
|
ENST00000466955.5:n.477T=
|
|
|
ENST00000468709.5:n.792T=
|
|
|
ENST00000478047.1:n.1199+7594T=
|
|
|
ENST00000482452.5:n.624T=
|
|
|
ENST00000496796.5:n.700T=
|
|
|
NM_001303404.1:c.936T=
|
NP_001290333.1:p.Ser312=
|
|
NM_001303405.1:c.525T=
|
NP_001290334.1:p.Ser175=
|
|
NM_001303406.1:c.525T=
|
NP_001290335.1:p.Ser175=
|
|
NM_001303407.1:c.201T=
|
NP_001290336.1:p.Ser67=
|
|
NM_018294.5:c.936T=
|
NP_060764.3:p.Ser312=
|
|
NM_018294.6:c.936T=
MANE Select
|
NP_060764.3:p.Ser312=
|
|
NM_001303404.2:c.936T=
|
NP_001290333.1:p.Ser312=
|
|
NM_001303405.2:c.525T=
|
NP_001290334.1:p.Ser175=
|
|
NM_001303406.2:c.525T=
|
NP_001290335.1:p.Ser175=
|
|
NM_001303407.2:c.201T=
|
NP_001290336.1:p.Ser67=
|
|