ENST00000265594.9:c.1412T>G
MANE Select
|
ENSP00000265594.4:p.Leu471Arg
|
|
ENST00000265594.8:c.1412T>G
|
ENSP00000265594.4:p.Leu471Arg
|
|
ENST00000476176.5:c.1271T>G
|
ENSP00000420433.1:p.Leu424Arg
|
|
ENST00000492597.5:c.1085T>G
|
ENSP00000419898.1:p.Leu362Arg
|
|
ENST00000495767.5:c.*993T>G
|
ENSP00000419658.1:n.*993T>G
|
|
ENST00000497830.5:c.*1009T>G
|
ENSP00000420088.1:n.*1009T>G
|
|
ENST00000497959.5:c.1263+1626T>G
|
ENSP00000420648.1:n.1263+1626T>G
|
|
ENST00000539926.5:c.962T>G
|
ENSP00000441253.2:p.Leu321Arg
|
|
ENST00000610757.4:c.962T>G
|
ENSP00000480435.1:p.Leu321Arg
|
|
ENST00000629669.2:c.1263+1626T>G
|
ENSP00000486824.1:n.1263+1626T>G
|
|
NM_001293273.1:c.1061T>G
|
NP_001280202.1:p.Leu354Arg
|
|
NM_020166.4:c.1412T>G
|
NP_064551.3:p.Leu471Arg
|
|
NR_120639.1:n.1326T>G
|
|
|
NR_120640.1:n.2044+1626T>G
|
|
|
XM_006713702.1:c.1085T>G
|
XP_006713765.1:p.Leu362Arg
|
|
XM_011512992.1:c.1298T>G
|
XP_011511294.1:p.Leu433Arg
|
|
XM_011512993.1:c.1377+1626T>G
|
XP_011511295.1:n.1377+1626T>G
|
|
XR_241502.2:n.1524+1626T>G
|
|
|
XR_924159.1:n.1559T>G
|
|
|
NM_001363880.1:c.1085T>G
|
NP_001350809.1:p.Leu362Arg
|
|
XM_011512992.2:c.1298T>G
|
XP_011511294.1:p.Leu433Arg
|
|
XR_001740207.2:n.1535T>G
|
|
|
XR_001740208.2:n.1535T>G
|
|
|
XR_001740209.2:n.1470+1626T>G
|
|
|
XR_001740210.1:n.1365T>G
|
|
|
XR_002959553.1:n.1535T>G
|
|
|
XR_002959554.1:n.1500+1626T>G
|
|
|
XR_241502.3:n.1470+1626T>G
|
|
|
NM_020166.5:c.1412T>G
MANE Select
|
NP_064551.3:p.Leu471Arg
|
|
NM_001293273.2:c.1061T>G
|
NP_001280202.1:p.Leu354Arg
|
|
NR_120639.2:n.1235T>G
|
|
|
NR_120640.2:n.2044+1626T>G
|
|
|