ENST00000327047.6:c.*1069T>C
MANE Select
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ENSP00000322280.1:n.*1069T>C
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ENST00000295911.6:c.348T>C
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ENSP00000295911.2:p.Thr116=
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ENST00000327047.5:c.*1069T>C
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ENSP00000322280.1:n.*1069T>C
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ENST00000562308.5:c.104+14715T>C
|
|
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ENST00000565169.1:c.162+14715T>C
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|
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ENST00000569170.5:c.162+14715T>C
|
|
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NM_001195794.1:c.*1069T>C , LRG_700t1:c.*1069T>C
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NP_001182723.1:n.*1069T>C
|
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NM_001256819.1:c.*1382T>C
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NP_001243748.1:n.*1382T>C
|
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NM_052995.2:c.348T>C , LRG_700t2:c.348T>C
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NP_443721.1:p.Thr116=
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NM_174878.2:c.*1069T>C
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NP_777367.1:n.*1069T>C
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NR_046380.2:n.2249T>C
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|
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XR_924167.1:n.2080T>C
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|
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NM_001256819.2:c.*1382T>C
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NP_001243748.1:n.*1382T>C
|
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NM_174878.3:c.*1069T>C
MANE Select
|
NP_777367.1:n.*1069T>C
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NR_046380.3:n.1977T>C
|
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