ENST00000610179.7:c.961T>A
MANE Select
|
ENSP00000477429.2:p.Phe321Ile
|
|
ENST00000316562.9:c.1291T>A
|
ENSP00000313377.4:p.Phe431Ile
|
|
ENST00000336066.8:c.*302T>A
|
ENSP00000477229.2:n.*302T>A
|
|
ENST00000610179.6:c.961T>A
|
ENSP00000477429.2:p.Phe321Ile
|
|
ENST00000643504.2:c.*591T>A
|
ENSP00000495157.2:n.*591T>A
|
|
ENST00000646394.1:c.788T>A
|
|
|
ENST00000316562.8:c.1291T>A
|
ENSP00000313377.4:p.Phe431Ile
|
|
ENST00000336066.7:c.*302T>A
|
ENSP00000477229.1:n.*302T>A
|
|
ENST00000464452.1:n.526T>A
|
|
|
ENST00000495692.5:c.-18T>A
|
ENSP00000476745.1:n.-18T>A
|
|
ENST00000497424.5:c.418T>A
|
ENSP00000417609.1:p.Phe140Ile
|
|
ENST00000610179.5:c.922T>A
|
ENSP00000477429.1:p.Phe308Ile
|
|
ENST00000621507.1:c.418T>A
|
ENSP00000481523.1:p.Phe140Ile
|
|
NM_024960.4:c.418T>A
|
NP_079236.3:p.Phe140Ile
|
|
NM_153638.2:c.1291T>A
|
NP_705902.2:p.Phe431Ile
|
|
NM_153640.2:c.418T>A
|
NP_705904.1:p.Phe140Ile
|
|
XM_005260835.2:c.676T>A
|
XP_005260892.1:p.Phe226Ile
|
|
XM_005260836.3:c.418T>A
|
XP_005260893.3:p.Phe140Ile
|
|
XM_006723631.1:c.418T>A
|
XP_006723694.1:p.Phe140Ile
|
|
XM_011529364.1:c.1235+1683T>A
|
XP_011527666.1:n.1235+1683T>A
|
|
NM_001324191.1:c.418T>A
|
NP_001311120.1:p.Phe140Ile
|
|
NM_001324193.1:c.-18T>A
|
NP_001311122.1:n.-18T>A
|
|
NM_024960.5:c.418T>A
|
NP_079236.3:p.Phe140Ile
|
|
NM_153638.3:c.1291T>A
|
NP_705902.2:p.Phe431Ile
|
|
NM_153640.3:c.418T>A
|
NP_705904.1:p.Phe140Ile
|
|
NR_136715.1:n.1315T>A
|
|
|
XM_005260835.3:c.676T>A
|
XP_005260892.1:p.Phe226Ile
|
|
XM_005260836.4:c.418T>A
|
XP_005260893.3:p.Phe140Ile
|
|
XM_011529364.3:c.1235+1683T>A
|
XP_011527666.1:n.1235+1683T>A
|
|
XM_017028077.2:c.-18T>A
|
XP_016883566.1:n.-18T>A
|
|
XM_017028078.2:c.-18T>A
|
XP_016883567.1:n.-18T>A
|
|
XM_017028079.2:c.-18T>A
|
XP_016883568.1:n.-18T>A
|
|
XM_024452002.1:c.-18T>A
|
XP_024307770.1:n.-18T>A
|
|
XR_002958533.1:n.2079T>A
|
|
|
NM_001324191.2:c.418T>A
|
NP_001311120.1:p.Phe140Ile
|
|
NM_001324193.2:c.-18T>A
|
NP_001311122.1:n.-18T>A
|
|
NM_024960.6:c.418T>A
|
NP_079236.3:p.Phe140Ile
|
|
NR_136715.2:n.862T>A
|
|
|
NM_001386393.1:c.961T>A
MANE Select
|
NP_001373322.1:p.Phe321Ile
|
|
NM_153638.4:c.1291T>A
|
NP_705902.2:p.Phe431Ile
|
|
NM_153640.4:c.418T>A
|
NP_705904.1:p.Phe140Ile
|
|