ENST00000265594.9:c.1518G>T
MANE Select
|
ENSP00000265594.4:p.Glu506Asp
|
|
ENST00000265594.8:c.1518G>T
|
ENSP00000265594.4:p.Glu506Asp
|
|
ENST00000476176.5:c.1377G>T
|
ENSP00000420433.1:p.Glu459Asp
|
|
ENST00000489909.1:n.62G>T
|
|
|
ENST00000492597.5:c.1191G>T
|
ENSP00000419898.1:p.Glu397Asp
|
|
ENST00000495767.5:c.*1099G>T
|
ENSP00000419658.1:n.*1099G>T
|
|
ENST00000497830.5:c.*1115G>T
|
ENSP00000420088.1:n.*1115G>T
|
|
ENST00000497959.5:c.1263+1732G>T
|
ENSP00000420648.1:n.1263+1732G>T
|
|
ENST00000539926.5:c.1068G>T
|
ENSP00000441253.2:p.Glu356Asp
|
|
ENST00000610757.4:c.1068G>T
|
ENSP00000480435.1:p.Glu356Asp
|
|
ENST00000629669.2:c.1263+1732G>T
|
ENSP00000486824.1:n.1263+1732G>T
|
|
NM_001293273.1:c.1167G>T
|
NP_001280202.1:p.Glu389Asp
|
|
NM_020166.4:c.1518G>T
|
NP_064551.3:p.Glu506Asp
|
|
NR_120639.1:n.1432G>T
|
|
|
NR_120640.1:n.2044+1732G>T
|
|
|
XM_006713702.1:c.1191G>T
|
XP_006713765.1:p.Glu397Asp
|
|
XM_011512992.1:c.1404G>T
|
XP_011511294.1:p.Glu468Asp
|
|
XM_011512993.1:c.1377+1732G>T
|
XP_011511295.1:n.1377+1732G>T
|
|
XR_241502.2:n.1524+1732G>T
|
|
|
XR_924159.1:n.1665G>T
|
|
|
NM_001363880.1:c.1191G>T
|
NP_001350809.1:p.Glu397Asp
|
|
XM_011512992.2:c.1404G>T
|
XP_011511294.1:p.Glu468Asp
|
|
XR_001740207.2:n.1641G>T
|
|
|
XR_001740208.2:n.1641G>T
|
|
|
XR_001740209.2:n.1470+1732G>T
|
|
|
XR_001740210.1:n.1471G>T
|
|
|
XR_002959553.1:n.1641G>T
|
|
|
XR_002959554.1:n.1500+1732G>T
|
|
|
XR_241502.3:n.1470+1732G>T
|
|
|
NM_020166.5:c.1518G>T
MANE Select
|
NP_064551.3:p.Glu506Asp
|
|
NM_001293273.2:c.1167G>T
|
NP_001280202.1:p.Glu389Asp
|
|
NR_120639.2:n.1341G>T
|
|
|
NR_120640.2:n.2044+1732G>T
|
|
|