ENST00000375128.5:c.772C>T
MANE Select
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ENSP00000364270.5:p.Arg258Cys
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|
ENST00000375128.4:c.772C>T
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ENSP00000364270.4:p.Arg258Cys
|
|
ENST00000462523.5:c.*208C>T
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ENSP00000433006.1:n.*208C>T
|
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ENST00000485042.1:n.284C>T
|
|
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NM_000380.3:c.772C>T , LRG_471t1:c.772C>T
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NP_000371.1:p.Arg258Cys
|
|
NR_027302.1:n.1120C>T
|
|
|
XM_006717278.1:c.772C>T
|
XP_006717341.1:p.Pro258Ser
|
|
XM_011518988.1:c.772C>T
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XP_011517290.1:p.Arg258Cys
|
|
NM_001354975.1:c.646C>T
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NP_001341904.1:p.Arg216Cys
|
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NR_149091.1:n.617C>T
|
|
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NR_149092.1:n.783C>T
|
|
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NR_149093.1:n.1309C>T
|
|
|
NR_149094.1:n.1203C>T
|
|
|
NM_000380.4:c.772C>T
MANE Select
|
NP_000371.1:p.Arg258Cys
|
|
NM_001354975.2:c.646C>T
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NP_001341904.1:p.Arg216Cys
|
|
NR_027302.2:n.1051C>T
|
|
|
NR_149091.2:n.548C>T
|
|
|
NR_149092.2:n.714C>T
|
|
|
NR_149093.2:n.1240C>T
|
|
|
NR_149094.2:n.1134C>T
|
|
|