ENST00000265512.12:c.1126A>T
MANE Select
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ENSP00000265512.7:p.Thr376Ser
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ENST00000265512.11:c.1126A>T
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ENSP00000265512.7:p.Thr376Ser
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ENST00000505590.5:c.1183A>T
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ENSP00000425416.1:p.Thr395Ser
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ENST00000508393.5:c.1183A>T
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ENSP00000424630.1:p.Thr395Ser
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ENST00000509471.5:c.480A>T
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ENSP00000424583.1:n.480A>T
|
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ENST00000629236.2:c.1126A>T
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ENSP00000486450.1:p.Thr376Ser
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NM_000670.3:c.1126A>T
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NP_000661.2:p.Thr376Ser
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NM_000670.4:c.1126A>T
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NP_000661.2:p.Thr376Ser
|
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NM_001306171.1:c.1183A>T
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NP_001293100.1:p.Thr395Ser
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NM_001306172.1:c.1183A>T
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NP_001293101.1:p.Thr395Ser
|
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NR_037884.1:n.429-9096T>A
|
|
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XR_938685.1:n.1465A>T
|
|
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XR_938686.1:n.1456A>T
|
|
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XR_938687.1:n.1329A>T
|
|
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NM_000670.5:c.1126A>T
MANE Select
|
NP_000661.2:p.Thr376Ser
|
|
NM_001306171.2:c.1183A>T
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NP_001293100.1:p.Thr395Ser
|
|
NM_001306172.2:c.1183A>T
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NP_001293101.1:p.Thr395Ser
|
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