ENST00000205402.10:c.1402G>A
MANE Select
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ENSP00000205402.3:p.Ala468Thr
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ENST00000205402.9:c.1402G>A
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ENSP00000205402.3:p.Ala468Thr
|
|
ENST00000415325.5:c.*1076G>A
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ENSP00000402593.1:n.*1076G>A
|
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ENST00000417551.5:c.1402G>A
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ENSP00000390667.1:p.Ala468Thr
|
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ENST00000437604.6:c.1258G>A
|
ENSP00000387542.2:p.Ala420Thr
|
|
ENST00000440410.5:c.1333G>A
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ENSP00000417016.1:p.Ala445Thr
|
|
NM_000108.4:c.1402G>A
|
NP_000099.2:p.Ala468Thr
|
|
NM_001289750.1:c.1105G>A
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NP_001276679.1:p.Ala369Thr
|
|
NM_001289751.1:c.1333G>A
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NP_001276680.1:p.Ala445Thr
|
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NM_001289752.1:c.1258G>A
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NP_001276681.1:p.Ala420Thr
|
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NM_000108.5:c.1402G>A
MANE Select
|
NP_000099.2:p.Ala468Thr
|
|