ENST00000356231.4:c.1834G>A
MANE Select
|
ENSP00000348564.3:p.Asp612Asn
|
|
ENST00000643434.1:c.*1012G>A
|
ENSP00000494699.1:n.*1012G>A
|
|
ENST00000356231.3:c.1834G>A
|
ENSP00000348564.3:p.Asp612Asn
|
|
NM_138477.2:c.1834G>A
|
NP_612486.2:p.Asp612Asn
|
|
XM_005254176.3:c.1837G>A
|
XP_005254233.1:p.Asp613Asn
|
|
XM_011521270.1:c.1861G>A
|
XP_011519572.1:p.Asp621Asn
|
|
XM_011521271.1:c.1858G>A
|
XP_011519573.1:p.Asp620Asn
|
|
XM_011521272.1:c.1861G>A
|
XP_011519574.1:p.Asp621Asn
|
|
XM_011521273.1:c.1861G>A
|
XP_011519575.1:p.Asp621Asn
|
|
XM_011521274.1:c.826G>A
|
XP_011519576.1:p.Asp276Asn
|
|
XM_011521275.1:c.1078G>A
|
XP_011519577.1:p.Asp360Asn
|
|
XR_931757.1:n.1872G>A
|
|
|
NM_138477.4:c.1834G>A
MANE Select
|
NP_612486.2:p.Asp612Asn
|
|
XM_005254176.5:c.1837G>A
|
XP_005254233.1:p.Asp613Asn
|
|
XM_011521270.2:c.1861G>A
|
XP_011519572.1:p.Asp621Asn
|
|
XM_011521271.2:c.1858G>A
|
XP_011519573.1:p.Asp620Asn
|
|
XM_011521274.2:c.826G>A
|
XP_011519576.1:p.Asp276Asn
|
|
XR_001751104.1:n.1891G>A
|
|
|
XR_001751105.1:n.1891G>A
|
|
|
XR_931757.2:n.1892G>A
|
|
|