ENST00000261769.10:c.2521G>T
MANE Select
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ENSP00000261769.4:p.Glu841Ter
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ENST00000261769.9:c.2521G>T
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ENSP00000261769.4:p.Glu841Ter
|
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ENST00000422392.6:c.2338G>T
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ENSP00000414946.2:p.Glu780Ter
|
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ENST00000562118.1:n.739G>T
|
|
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ENST00000562836.5:n.2592G>T
|
|
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ENST00000566510.5:c.*1187G>T
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ENSP00000458139.1:n.*1187G>T
|
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ENST00000566612.5:c.*761G>T
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ENSP00000454782.1:n.*761G>T
|
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ENST00000611625.4:c.2584G>T
|
ENSP00000481063.1:p.Glu862Ter
|
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ENST00000612417.4:c.1854-820G>T
|
ENSP00000478360.1:n.1854-820G>T
|
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ENST00000621016.4:c.1866-832G>T
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ENSP00000480664.1:n.1866-832G>T
|
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NM_004360.3:c.2521G>T , LRG_301t1:c.2521G>T
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NP_004351.1:p.Glu841Ter
|
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XM_011523488.1:c.1786G>T
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XP_011521790.1:p.Glu596Ter
|
|
XM_011523489.1:c.1786G>T
|
XP_011521791.1:p.Glu596Ter
|
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NM_001317184.1:c.2338G>T
|
NP_001304113.1:p.Glu780Ter
|
|
NM_001317185.1:c.973G>T
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NP_001304114.1:p.Glu325Ter
|
|
NM_001317186.1:c.556G>T
|
NP_001304115.1:p.Glu186Ter
|
|
NM_004360.4:c.2521G>T
|
NP_004351.1:p.Glu841Ter
|
|
NM_004360.5:c.2521G>T
MANE Select
|
NP_004351.1:p.Glu841Ter
|
|
NM_001317184.2:c.2338G>T
|
NP_001304113.1:p.Glu780Ter
|
|
NM_001317185.2:c.973G>T
|
NP_001304114.1:p.Glu325Ter
|
|
NM_001317186.2:c.556G>T
|
NP_001304115.1:p.Glu186Ter
|
|