ENST00000366930.9:c.958C>T
MANE Select
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ENSP00000355897.4:p.Arg320Cys
|
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ENST00000366929.4:c.1042C>T
|
ENSP00000355896.4:p.Arg348Cys
|
|
ENST00000366930.8:c.958C>T
|
ENSP00000355897.4:p.Arg320Cys
|
|
ENST00000479322.1:n.442C>T
|
|
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NM_001135599.2:c.1042C>T
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NP_001129071.1:p.Arg348Cys
|
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NM_003238.3:c.958C>T
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NP_003229.1:p.Arg320Cys
|
|
NM_001135599.3:c.1042C>T
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NP_001129071.1:p.Arg348Cys
|
|
NM_003238.4:c.958C>T
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NP_003229.1:p.Arg320Cys
|
|
NR_138148.1:n.2261C>T
|
|
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NR_138149.1:n.2345C>T
|
|
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NM_003238.5:c.958C>T
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NP_003229.1:p.Arg320Cys
|
|
NM_003238.6:c.958C>T
MANE Select
|
NP_003229.1:p.Arg320Cys
|
|
NM_001135599.4:c.1042C>T
|
NP_001129071.1:p.Arg348Cys
|
|
NR_138148.2:n.2209C>T
|
|
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NR_138149.2:n.2293C>T
|
|
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