ENST00000278407.9:c.1430T>C
MANE Select
|
ENSP00000278407.4:p.Phe477Ser
|
|
ENST00000528996.2:c.*327T>C
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ENSP00000431226.2:n.*327T>C
|
|
ENST00000531605.2:c.*1206T>C
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ENSP00000503752.1:n.*1206T>C
|
|
ENST00000619430.2:c.1226T>C
|
ENSP00000478572.2:p.Phe409Ser
|
|
ENST00000676670.1:c.1430T>C
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ENSP00000504807.1:p.Phe477Ser
|
|
ENST00000676741.1:n.2512T>C
|
|
|
ENST00000677624.1:c.*850T>C
|
ENSP00000503979.1:n.*850T>C
|
|
ENST00000677625.1:c.1376T>C
|
ENSP00000502857.1:p.Phe459Ser
|
|
ENST00000677856.1:n.1683T>C
|
|
|
ENST00000677915.1:c.*327T>C
|
ENSP00000503118.1:n.*327T>C
|
|
ENST00000678533.1:c.*984T>C
|
ENSP00000503873.1:n.*984T>C
|
|
ENST00000678592.1:c.*370T>C
|
ENSP00000504424.1:n.*370T>C
|
|
ENST00000278407.8:c.1430T>C
|
ENSP00000278407.4:p.Phe477Ser
|
|
ENST00000340687.10:c.1319T>C
|
ENSP00000341861.6:p.Phe440Ser
|
|
ENST00000378323.8:c.1445T>C
|
ENSP00000367574.4:p.Phe482Ser
|
|
ENST00000378324.6:c.1274T>C
|
ENSP00000367575.2:p.Phe425Ser
|
|
ENST00000403558.1:c.1559T>C
|
ENSP00000384420.1:p.Phe520Ser
|
|
ENST00000528996.1:c.631T>C
|
ENSP00000431226.1:n.631T>C
|
|
ENST00000530113.1:n.887T>C
|
|
|
ENST00000531133.5:c.931T>C
|
ENSP00000435431.1:n.931T>C
|
|
ENST00000531797.5:c.*455T>C
|
ENSP00000432554.1:n.*455T>C
|
|
ENST00000619430.1:c.561T>C
|
ENSP00000478572.1:n.561T>C
|
|
NM_000062.2:c.1430T>C , LRG_105t1:c.1430T>C
|
NP_000053.2:p.Phe477Ser
|
|
NM_001032295.1:c.1430T>C
|
NP_001027466.1:p.Phe477Ser
|
|
NM_000062.3:c.1430T>C
MANE Select
|
NP_000053.2:p.Phe477Ser
|
|
NM_001032295.2:c.1430T>C
|
NP_001027466.1:p.Phe477Ser
|
|