ENST00000278407.9:c.1498G>T
MANE Select
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ENSP00000278407.4:p.Ala500Ser
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ENST00000528996.2:c.*395G>T
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ENSP00000431226.2:n.*395G>T
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ENST00000531605.2:c.*1274G>T
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ENSP00000503752.1:n.*1274G>T
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ENST00000619430.2:c.1294G>T
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ENSP00000478572.2:p.Ala432Ser
|
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ENST00000676670.1:c.1498G>T
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ENSP00000504807.1:p.Ala500Ser
|
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ENST00000676741.1:n.2580G>T
|
|
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ENST00000677624.1:c.*918G>T
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ENSP00000503979.1:n.*918G>T
|
|
ENST00000677625.1:c.1444G>T
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ENSP00000502857.1:p.Ala482Ser
|
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ENST00000677856.1:n.1751G>T
|
|
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ENST00000677915.1:c.*395G>T
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ENSP00000503118.1:n.*395G>T
|
|
ENST00000678533.1:c.*1052G>T
|
ENSP00000503873.1:n.*1052G>T
|
|
ENST00000678592.1:c.*438G>T
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ENSP00000504424.1:n.*438G>T
|
|
ENST00000278407.8:c.1498G>T
|
ENSP00000278407.4:p.Ala500Ser
|
|
ENST00000340687.10:c.1387G>T
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ENSP00000341861.6:p.Ala463Ser
|
|
ENST00000378323.8:c.1513G>T
|
ENSP00000367574.4:p.Ala505Ser
|
|
ENST00000378324.6:c.1342G>T
|
ENSP00000367575.2:p.Ala448Ser
|
|
ENST00000403558.1:c.1627G>T
|
ENSP00000384420.1:p.Ala543Ser
|
|
ENST00000528996.1:c.699G>T
|
ENSP00000431226.1:n.699G>T
|
|
ENST00000531133.5:c.999G>T
|
ENSP00000435431.1:n.999G>T
|
|
ENST00000531797.5:c.*523G>T
|
ENSP00000432554.1:n.*523G>T
|
|
ENST00000619430.1:c.629G>T
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ENSP00000478572.1:n.629G>T
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|
NM_000062.2:c.1498G>T , LRG_105t1:c.1498G>T
|
NP_000053.2:p.Ala500Ser
|
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NM_001032295.1:c.1498G>T
|
NP_001027466.1:p.Ala500Ser
|
|
NM_000062.3:c.1498G>T
MANE Select
|
NP_000053.2:p.Ala500Ser
|
|
NM_001032295.2:c.1498G>T
|
NP_001027466.1:p.Ala500Ser
|
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