ENST00000375128.5:c.769T>A
MANE Select
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ENSP00000364270.5:p.Tyr257Asn
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ENST00000375128.4:c.769T>A
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ENSP00000364270.4:p.Tyr257Asn
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ENST00000462523.5:c.*205T>A
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ENSP00000433006.1:n.*205T>A
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ENST00000485042.1:n.281T>A
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|
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NM_000380.3:c.769T>A , LRG_471t1:c.769T>A
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NP_000371.1:p.Tyr257Asn
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NR_027302.1:n.1117T>A
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|
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XM_006717278.1:c.769T>A
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XP_006717341.1:p.Tyr257Asn
|
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XM_011518988.1:c.769T>A
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XP_011517290.1:p.Tyr257Asn
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NM_001354975.1:c.643T>A
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NP_001341904.1:p.Tyr215Asn
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NR_149091.1:n.614T>A
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|
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NR_149092.1:n.780T>A
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|
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NR_149093.1:n.1306T>A
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|
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NR_149094.1:n.1200T>A
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|
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NM_000380.4:c.769T>A
MANE Select
|
NP_000371.1:p.Tyr257Asn
|
|
NM_001354975.2:c.643T>A
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NP_001341904.1:p.Tyr215Asn
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NR_027302.2:n.1048T>A
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|
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NR_149091.2:n.545T>A
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|
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NR_149092.2:n.711T>A
|
|
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NR_149093.2:n.1237T>A
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|
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NR_149094.2:n.1131T>A
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