ENST00000355832.10:c.3388T>A
MANE Select
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ENSP00000348089.5:p.Ser1130Thr
|
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ENST00000679552.1:n.459T>A
|
|
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ENST00000679871.1:n.534T>A
|
|
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ENST00000679974.1:n.437T>A
|
|
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ENST00000681632.1:n.4791T>A
|
|
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ENST00000681659.1:c.3229T>A
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ENSP00000505631.1:p.Ser1077Thr
|
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ENST00000355832.9:c.3388T>A
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ENSP00000348089.5:p.Ser1130Thr
|
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ENST00000623073.3:c.*1684T>A
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ENSP00000485650.1:n.*1684T>A
|
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ENST00000623115.3:c.1498T>A
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ENSP00000485321.1:p.Ser500Thr
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ENST00000624341.3:c.1220T>A
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|
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NM_000124.3:c.3388T>A
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NP_000115.1:p.Ser1130Thr
|
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XR_945953.1:n.243-993A>T
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|
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NM_001346440.1:c.3388T>A
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NP_001333369.1:p.Ser1130Thr
|
|
NM_000124.4:c.3388T>A
MANE Select
|
NP_000115.1:p.Ser1130Thr
|
|
NM_001346440.2:c.3388T>A
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NP_001333369.1:p.Ser1130Thr
|
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