ENST00000265512.12:c.938A>T
MANE Select
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ENSP00000265512.7:p.Glu313Val
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ENST00000265512.11:c.938A>T
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ENSP00000265512.7:p.Glu313Val
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ENST00000505590.5:c.995A>T
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ENSP00000425416.1:p.Glu332Val
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ENST00000506705.5:c.*912A>T
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ENSP00000426667.1:n.*912A>T
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ENST00000508393.5:c.995A>T
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ENSP00000424630.1:p.Glu332Val
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ENST00000509471.5:c.334-518A>T
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ENSP00000424583.1:n.334-518A>T
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ENST00000629236.2:c.938A>T
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ENSP00000486450.1:p.Glu313Val
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NM_000670.3:c.938A>T
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NP_000661.2:p.Glu313Val
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NM_000670.4:c.938A>T
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NP_000661.2:p.Glu313Val
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NM_001306171.1:c.995A>T
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NP_001293100.1:p.Glu332Val
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NM_001306172.1:c.995A>T
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NP_001293101.1:p.Glu332Val
|
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NR_037884.1:n.429-6305T>A
|
|
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XR_938685.1:n.1166A>T
|
|
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XR_938686.1:n.1157A>T
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|
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XR_938687.1:n.1030A>T
|
|
|
NM_000670.5:c.938A>T
MANE Select
|
NP_000661.2:p.Glu313Val
|
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NM_001306171.2:c.995A>T
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NP_001293100.1:p.Glu332Val
|
|
NM_001306172.2:c.995A>T
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NP_001293101.1:p.Glu332Val
|
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