ENST00000265594.9:c.1273G>T
MANE Select
|
ENSP00000265594.4:p.Glu425Ter
|
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ENST00000265594.8:c.1273G>T
|
ENSP00000265594.4:p.Glu425Ter
|
|
ENST00000476176.5:c.1132G>T
|
ENSP00000420433.1:p.Glu378Ter
|
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ENST00000492597.5:c.946G>T
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ENSP00000419898.1:p.Glu316Ter
|
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ENST00000495767.5:c.*854G>T
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ENSP00000419658.1:n.*854G>T
|
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ENST00000497830.5:c.*870G>T
|
ENSP00000420088.1:n.*870G>T
|
|
ENST00000497959.5:c.1159G>T
|
ENSP00000420648.1:p.Glu387Ter
|
|
ENST00000539926.5:c.823G>T
|
ENSP00000441253.2:p.Glu275Ter
|
|
ENST00000610757.4:c.823G>T
|
ENSP00000480435.1:p.Glu275Ter
|
|
ENST00000629669.2:c.1159G>T
|
ENSP00000486824.1:p.Glu387Ter
|
|
NM_001293273.1:c.922G>T
|
NP_001280202.1:p.Glu308Ter
|
|
NM_020166.4:c.1273G>T
|
NP_064551.3:p.Glu425Ter
|
|
NR_120639.1:n.1187G>T
|
|
|
NR_120640.1:n.1940G>T
|
|
|
XM_006713702.1:c.946G>T
|
XP_006713765.1:p.Glu316Ter
|
|
XM_011512992.1:c.1159G>T
|
XP_011511294.1:p.Glu387Ter
|
|
XM_011512993.1:c.1273G>T
|
XP_011511295.1:p.Glu425Ter
|
|
XR_241502.2:n.1420G>T
|
|
|
XR_924159.1:n.1420G>T
|
|
|
NM_001363880.1:c.946G>T
|
NP_001350809.1:p.Glu316Ter
|
|
XM_011512992.2:c.1159G>T
|
XP_011511294.1:p.Glu387Ter
|
|
XR_001740207.2:n.1396G>T
|
|
|
XR_001740208.2:n.1396G>T
|
|
|
XR_001740209.2:n.1366G>T
|
|
|
XR_001740210.1:n.1226G>T
|
|
|
XR_002959553.1:n.1396G>T
|
|
|
XR_002959554.1:n.1396G>T
|
|
|
XR_241502.3:n.1366G>T
|
|
|
NM_020166.5:c.1273G>T
MANE Select
|
NP_064551.3:p.Glu425Ter
|
|
NM_001293273.2:c.922G>T
|
NP_001280202.1:p.Glu308Ter
|
|
NR_120639.2:n.1096G>T
|
|
|
NR_120640.2:n.1940G>T
|
|
|