ENST00000356231.4:c.3481C>A
MANE Select
|
ENSP00000348564.3:p.Leu1161Met
|
|
ENST00000643434.1:c.*2548C>A
|
ENSP00000494699.1:n.*2548C>A
|
|
ENST00000356231.3:c.3481C>A
|
ENSP00000348564.3:p.Leu1161Met
|
|
ENST00000562465.5:c.1427C>A
|
ENSP00000454246.1:n.1427C>A
|
|
ENST00000563604.1:n.417C>A
|
|
|
ENST00000565930.1:n.82C>A
|
|
|
NM_138477.2:c.3481C>A
|
NP_612486.2:p.Leu1161Met
|
|
XM_005254176.3:c.3484C>A
|
XP_005254233.1:p.Leu1162Met
|
|
XM_011521270.1:c.3508C>A
|
XP_011519572.1:p.Leu1170Met
|
|
XM_011521271.1:c.3505C>A
|
XP_011519573.1:p.Leu1169Met
|
|
XM_011521274.1:c.2473C>A
|
XP_011519576.1:p.Leu825Met
|
|
XM_011521275.1:c.2725C>A
|
XP_011519577.1:p.Leu909Met
|
|
NM_138477.4:c.3481C>A
MANE Select
|
NP_612486.2:p.Leu1161Met
|
|
XM_005254176.5:c.3484C>A
|
XP_005254233.1:p.Leu1162Met
|
|
XM_011521270.2:c.3508C>A
|
XP_011519572.1:p.Leu1170Met
|
|
XM_011521271.2:c.3505C>A
|
XP_011519573.1:p.Leu1169Met
|
|
XM_011521274.2:c.2473C>A
|
XP_011519576.1:p.Leu825Met
|
|
XR_001751104.1:n.3474C>A
|
|
|
XR_001751105.1:n.3491C>A
|
|
|