ENST00000673913.2:c.*132G>A
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ENSP00000501161.2:n.*132G>A
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ENST00000710286.1:c.2149G>A
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ENSP00000518176.1:p.Ala717Thr
|
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ENST00000673903.1:c.1417G>A
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ENSP00000501257.1:p.Ala473Thr
|
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ENST00000673913.1:c.642G>A
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ENSP00000501161.1:n.642G>A
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ENST00000302118.5:c.1792G>A
MANE Select
|
ENSP00000303208.5:p.Ala598Thr
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ENST00000490692.1:n.2338G>A
|
|
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NM_174936.3:c.1792G>A , LRG_275t1:c.1792G>A
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NP_777596.2:p.Ala598Thr
|
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NR_110451.1:n.1399G>A
|
|
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XM_011541193.1:c.913G>A
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XP_011539495.1:p.Ala305Thr
|
|
NM_174936.4:c.1792G>A
MANE Select
|
NP_777596.2:p.Ala598Thr
|
|
NR_110451.2:n.1399G>A
|
|
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