ENST00000375128.5:c.*66T>A
MANE Select
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ENSP00000364270.5:n.*66T>A
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|
ENST00000375128.4:c.*66T>A
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ENSP00000364270.4:n.*66T>A
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|
ENST00000462523.5:c.*324T>A
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ENSP00000433006.1:n.*324T>A
|
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ENST00000485042.1:n.400T>A
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|
|
NM_000380.3:c.*66T>A , LRG_471t1:c.*66T>A
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NP_000371.1:n.*66T>A
|
|
NR_027302.1:n.1236T>A
|
|
|
XM_006717278.1:c.772+116T>A
|
XP_006717341.1:n.772+116T>A
|
|
XM_011518988.1:c.772+116T>A
|
XP_011517290.1:n.772+116T>A
|
|
NM_001354975.1:c.*66T>A
|
NP_001341904.1:n.*66T>A
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|
NR_149091.1:n.733T>A
|
|
|
NR_149092.1:n.899T>A
|
|
|
NR_149093.1:n.1425T>A
|
|
|
NR_149094.1:n.1319T>A
|
|
|
NM_000380.4:c.*66T>A
MANE Select
|
NP_000371.1:n.*66T>A
|
|
NM_001354975.2:c.*66T>A
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NP_001341904.1:n.*66T>A
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|
NR_027302.2:n.1167T>A
|
|
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NR_149091.2:n.664T>A
|
|
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NR_149092.2:n.830T>A
|
|
|
NR_149093.2:n.1356T>A
|
|
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NR_149094.2:n.1250T>A
|
|
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