ENST00000436784.7:c.1496G>A
MANE Select
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ENSP00000389175.2:p.Gly499Glu
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ENST00000436784.6:c.1496G>A
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ENSP00000389175.2:p.Gly499Glu
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ENST00000461183.5:c.768G>A
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ENSP00000417264.1:p.Trp256Ter
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ENST00000471180.5:c.639G>A
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ENSP00000417526.1:p.Trp213Ter
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ENST00000473032.5:c.534G>A
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ENSP00000418951.1:p.Trp178Ter
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ENST00000486393.5:c.*859G>A
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ENSP00000419868.1:n.*859G>A
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ENST00000489173.1:n.1790G>A
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|
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NM_145262.3:c.1496G>A
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NP_660305.2:p.Gly499Glu
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NR_026699.1:n.1594G>A
|
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NR_026700.1:n.700G>A
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NR_026701.1:n.1592G>A
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NR_026702.1:n.630G>A
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XM_005264878.2:c.*615G>A
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XP_005264935.1:n.*615G>A
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XR_245095.2:n.2747G>A
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XM_017005730.1:c.1115G>A
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XP_016861219.1:p.Gly372Glu
|
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XM_024453351.1:c.1496G>A
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XP_024309119.1:p.Gly499Glu
|
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XM_024453352.1:c.*615G>A
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XP_024309120.1:n.*615G>A
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XR_001740022.2:n.3398G>A
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XR_001740023.2:n.2922G>A
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XR_245095.4:n.2748G>A
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NM_145262.4:c.1496G>A
MANE Select
|
NP_660305.2:p.Gly499Glu
|
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NR_026699.2:n.1586G>A
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|
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NR_026700.2:n.692G>A
|
|
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NR_026701.2:n.1584G>A
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NR_026702.2:n.622G>A
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NM_001144951.2:c.*615G>A
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NP_001138423.1:n.*615G>A
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