ENST00000265594.9:c.1522T>G
MANE Select
|
ENSP00000265594.4:p.Leu508Val
|
|
ENST00000265594.8:c.1522T>G
|
ENSP00000265594.4:p.Leu508Val
|
|
ENST00000476176.5:c.1381T>G
|
ENSP00000420433.1:p.Leu461Val
|
|
ENST00000489909.1:n.66T>G
|
|
|
ENST00000492597.5:c.1195T>G
|
ENSP00000419898.1:p.Leu399Val
|
|
ENST00000495767.5:c.*1103T>G
|
ENSP00000419658.1:n.*1103T>G
|
|
ENST00000497830.5:c.*1119T>G
|
ENSP00000420088.1:n.*1119T>G
|
|
ENST00000497959.5:c.1263+1736T>G
|
ENSP00000420648.1:n.1263+1736T>G
|
|
ENST00000539926.5:c.1072T>G
|
ENSP00000441253.2:p.Leu358Val
|
|
ENST00000610757.4:c.1072T>G
|
ENSP00000480435.1:p.Leu358Val
|
|
ENST00000629669.2:c.1263+1736T>G
|
ENSP00000486824.1:n.1263+1736T>G
|
|
NM_001293273.1:c.1171T>G
|
NP_001280202.1:p.Leu391Val
|
|
NM_020166.4:c.1522T>G
|
NP_064551.3:p.Leu508Val
|
|
NR_120639.1:n.1436T>G
|
|
|
NR_120640.1:n.2044+1736T>G
|
|
|
XM_006713702.1:c.1195T>G
|
XP_006713765.1:p.Leu399Val
|
|
XM_011512992.1:c.1408T>G
|
XP_011511294.1:p.Leu470Val
|
|
XM_011512993.1:c.1377+1736T>G
|
XP_011511295.1:n.1377+1736T>G
|
|
XR_241502.2:n.1524+1736T>G
|
|
|
XR_924159.1:n.1669T>G
|
|
|
NM_001363880.1:c.1195T>G
|
NP_001350809.1:p.Leu399Val
|
|
XM_011512992.2:c.1408T>G
|
XP_011511294.1:p.Leu470Val
|
|
XR_001740207.2:n.1645T>G
|
|
|
XR_001740208.2:n.1645T>G
|
|
|
XR_001740209.2:n.1470+1736T>G
|
|
|
XR_001740210.1:n.1475T>G
|
|
|
XR_002959553.1:n.1645T>G
|
|
|
XR_002959554.1:n.1500+1736T>G
|
|
|
XR_241502.3:n.1470+1736T>G
|
|
|
NM_020166.5:c.1522T>G
MANE Select
|
NP_064551.3:p.Leu508Val
|
|
NM_001293273.2:c.1171T>G
|
NP_001280202.1:p.Leu391Val
|
|
NR_120639.2:n.1345T>G
|
|
|
NR_120640.2:n.2044+1736T>G
|
|
|