ENST00000336079.8:c.1855A>C
MANE Select
|
ENSP00000336725.3:p.Ser619Arg
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ENST00000336079.7:c.1855A>C
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ENSP00000336725.3:p.Ser619Arg
|
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ENST00000360160.8:c.1855A>C
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ENSP00000353284.4:p.Ser619Arg
|
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NM_001122665.2:c.1855A>C
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NP_001116137.1:p.Ser619Arg
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NM_001302552.1:c.1846A>C
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NP_001289481.1:p.Ser616Arg
|
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NM_004660.4:c.1855A>C
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NP_004651.2:p.Ser619Arg
|
|
XM_006724878.1:c.1786A>C
|
XP_006724941.1:p.Ser596Arg
|
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NM_001122665.3:c.1855A>C
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NP_001116137.1:p.Ser619Arg
|
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NM_001302552.2:c.1846A>C
|
NP_001289481.1:p.Ser616Arg
|
|
NM_001324195.1:c.1786A>C
|
NP_001311124.1:p.Ser596Arg
|
|
NR_136716.1:n.2324A>C
|
|
|
NR_136717.1:n.2086A>C
|
|
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NR_136718.1:n.2404A>C
|
|
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NR_136719.1:n.2194A>C
|
|
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NR_136720.1:n.2255A>C
|
|
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NR_136721.1:n.1917A>C
|
|
|
NR_136722.1:n.2001A>C
|
|
|
NR_136723.1:n.2319A>C
|
|
|
NR_136724.1:n.2239A>C
|
|
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XR_001756014.2:n.2019A>C
|
|
|
NM_004660.5:c.1855A>C
MANE Select
|
NP_004651.2:p.Ser619Arg
|
|
NM_001302552.3:c.1846A>C
|
NP_001289481.1:p.Ser616Arg
|
|
NM_001324195.2:c.1786A>C
|
NP_001311124.1:p.Ser596Arg
|
|
NR_136716.2:n.2242A>C
|
|
|
NR_136717.2:n.2004A>C
|
|
|
NR_136718.2:n.2322A>C
|
|
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NR_136719.2:n.2112A>C
|
|
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NR_136720.2:n.2173A>C
|
|
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NR_136721.2:n.1907A>C
|
|
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