ENST00000375128.5:c.817A>T
MANE Select
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ENSP00000364270.5:p.Met273Leu
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|
ENST00000375128.4:c.817A>T
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ENSP00000364270.4:p.Met273Leu
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|
ENST00000462523.5:c.*253A>T
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ENSP00000433006.1:n.*253A>T
|
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ENST00000485042.1:n.329A>T
|
|
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NM_000380.3:c.817A>T , LRG_471t1:c.817A>T
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NP_000371.1:p.Met273Leu
|
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NR_027302.1:n.1165A>T
|
|
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XM_006717278.1:c.772+45A>T
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XP_006717341.1:n.772+45A>T
|
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XM_011518988.1:c.772+45A>T
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XP_011517290.1:n.772+45A>T
|
|
NM_001354975.1:c.691A>T
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NP_001341904.1:p.Met231Leu
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NR_149091.1:n.662A>T
|
|
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NR_149092.1:n.828A>T
|
|
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NR_149093.1:n.1354A>T
|
|
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NR_149094.1:n.1248A>T
|
|
|
NM_000380.4:c.817A>T
MANE Select
|
NP_000371.1:p.Met273Leu
|
|
NM_001354975.2:c.691A>T
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NP_001341904.1:p.Met231Leu
|
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NR_027302.2:n.1096A>T
|
|
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NR_149091.2:n.593A>T
|
|
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NR_149092.2:n.759A>T
|
|
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NR_149093.2:n.1285A>T
|
|
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NR_149094.2:n.1179A>T
|
|
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