ENST00000367590.9:c.327A>T
MANE Select
|
ENSP00000356562.4:p.Gln109His
|
|
ENST00000367589.3:c.327A>T
|
ENSP00000356561.3:p.Gln109His
|
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ENST00000367590.8:c.327A>T
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ENSP00000356562.4:p.Gln109His
|
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NM_001135669.1:c.327A>T
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NP_001129141.1:p.Gln109His
|
|
NM_004736.3:c.327A>T
|
NP_004727.2:p.Gln109His
|
|
NM_001328662.1:c.327A>T
|
NP_001315591.1:p.Gln109His
|
|
NR_137330.1:n.519A>T
|
|
|
NM_001135669.2:c.327A>T
|
NP_001129141.1:p.Gln109His
|
|
NM_001328662.2:c.327A>T
|
NP_001315591.1:p.Gln109His
|
|
NM_004736.4:c.327A>T
MANE Select
|
NP_004727.2:p.Gln109His
|
|
NR_137330.2:n.507A>T
|
|
|