ENST00000610179.7:c.931C>A
MANE Select
|
ENSP00000477429.2:p.Leu311Ile
|
|
ENST00000316562.9:c.1261C>A
|
ENSP00000313377.4:p.Leu421Ile
|
|
ENST00000336066.8:c.*272C>A
|
ENSP00000477229.2:n.*272C>A
|
|
ENST00000610179.6:c.931C>A
|
ENSP00000477429.2:p.Leu311Ile
|
|
ENST00000643504.2:c.*561C>A
|
ENSP00000495157.2:n.*561C>A
|
|
ENST00000646394.1:c.758C>A
|
|
|
ENST00000316562.8:c.1261C>A
|
ENSP00000313377.4:p.Leu421Ile
|
|
ENST00000336066.7:c.*272C>A
|
ENSP00000477229.1:n.*272C>A
|
|
ENST00000464452.1:n.496C>A
|
|
|
ENST00000495692.5:c.-48C>A
|
ENSP00000476745.1:n.-48C>A
|
|
ENST00000497424.5:c.388C>A
|
ENSP00000417609.1:p.Leu130Ile
|
|
ENST00000610179.5:c.892C>A
|
ENSP00000477429.1:p.Leu298Ile
|
|
ENST00000621507.1:c.388C>A
|
ENSP00000481523.1:p.Leu130Ile
|
|
NM_024960.4:c.388C>A
|
NP_079236.3:p.Leu130Ile
|
|
NM_153638.2:c.1261C>A
|
NP_705902.2:p.Leu421Ile
|
|
NM_153640.2:c.388C>A
|
NP_705904.1:p.Leu130Ile
|
|
XM_005260835.2:c.646C>A
|
XP_005260892.1:p.Leu216Ile
|
|
XM_005260836.3:c.388C>A
|
XP_005260893.3:p.Leu130Ile
|
|
XM_006723631.1:c.388C>A
|
XP_006723694.1:p.Leu130Ile
|
|
XM_011529364.1:c.1235+1653C>A
|
XP_011527666.1:n.1235+1653C>A
|
|
NM_001324191.1:c.388C>A
|
NP_001311120.1:p.Leu130Ile
|
|
NM_001324193.1:c.-48C>A
|
NP_001311122.1:n.-48C>A
|
|
NM_024960.5:c.388C>A
|
NP_079236.3:p.Leu130Ile
|
|
NM_153638.3:c.1261C>A
|
NP_705902.2:p.Leu421Ile
|
|
NM_153640.3:c.388C>A
|
NP_705904.1:p.Leu130Ile
|
|
NR_136715.1:n.1285C>A
|
|
|
XM_005260835.3:c.646C>A
|
XP_005260892.1:p.Leu216Ile
|
|
XM_005260836.4:c.388C>A
|
XP_005260893.3:p.Leu130Ile
|
|
XM_011529364.3:c.1235+1653C>A
|
XP_011527666.1:n.1235+1653C>A
|
|
XM_017028077.2:c.-48C>A
|
XP_016883566.1:n.-48C>A
|
|
XM_017028078.2:c.-48C>A
|
XP_016883567.1:n.-48C>A
|
|
XM_017028079.2:c.-48C>A
|
XP_016883568.1:n.-48C>A
|
|
XM_024452002.1:c.-48C>A
|
XP_024307770.1:n.-48C>A
|
|
XR_002958533.1:n.2049C>A
|
|
|
NM_001324191.2:c.388C>A
|
NP_001311120.1:p.Leu130Ile
|
|
NM_001324193.2:c.-48C>A
|
NP_001311122.1:n.-48C>A
|
|
NM_024960.6:c.388C>A
|
NP_079236.3:p.Leu130Ile
|
|
NR_136715.2:n.832C>A
|
|
|
NM_001386393.1:c.931C>A
MANE Select
|
NP_001373322.1:p.Leu311Ile
|
|
NM_153638.4:c.1261C>A
|
NP_705902.2:p.Leu421Ile
|
|
NM_153640.4:c.388C>A
|
NP_705904.1:p.Leu130Ile
|
|