ENST00000269217.11:c.1802A>C
MANE Plus Clinical
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ENSP00000269217.5:p.Glu601Ala
|
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ENST00000313654.14:c.6629A>C
MANE Select
|
ENSP00000324532.8:p.Glu2210Ala
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ENST00000649721.1:c.3521A>C
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ENSP00000497885.1:p.Glu1174Ala
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ENST00000269217.10:c.1802A>C
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ENSP00000269217.5:p.Glu601Ala
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ENST00000313654.13:c.6629A>C
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ENSP00000324532.8:p.Glu2210Ala
|
|
ENST00000399516.7:c.6461A>C
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ENSP00000382432.2:p.Glu2154Ala
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ENST00000586751.5:c.1407A>C
|
|
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ENST00000587184.5:c.1634A>C
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ENSP00000466557.1:p.Glu545Ala
|
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ENST00000588770.5:n.1207A>C
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|
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NM_000227.4:c.1802A>C
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NP_000218.3:p.Glu601Ala
|
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NM_001127717.2:c.6461A>C
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NP_001121189.2:p.Glu2154Ala
|
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NM_001127718.2:c.1634A>C
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NP_001121190.2:p.Glu545Ala
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NM_198129.2:c.6629A>C
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NP_937762.2:p.Glu2210Ala
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XM_011525978.1:c.6656A>C
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XP_011524280.1:p.Glu2219Ala
|
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XM_011525979.1:c.6647A>C
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XP_011524281.1:p.Glu2216Ala
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XM_011525980.1:c.6638A>C
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XP_011524282.1:p.Glu2213Ala
|
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XM_011525981.1:c.6524A>C
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XP_011524283.1:p.Glu2175Ala
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XM_011525982.1:c.6656A>C
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XP_011524284.1:p.Glu2219Ala
|
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XM_011525978.2:c.6656A>C
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XP_011524280.1:p.Glu2219Ala
|
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XM_011525979.2:c.6647A>C
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XP_011524281.1:p.Glu2216Ala
|
|
XM_011525980.2:c.6638A>C
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XP_011524282.1:p.Glu2213Ala
|
|
XM_011525981.2:c.6524A>C
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XP_011524283.1:p.Glu2175Ala
|
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XM_011525982.2:c.6656A>C
|
XP_011524284.1:p.Glu2219Ala
|
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XM_017025743.1:c.4508A>C
|
XP_016881232.1:p.Glu1503Ala
|
|
XM_017025744.1:c.2198A>C
|
XP_016881233.1:p.Glu733Ala
|
|
XR_001753199.1:n.6897A>C
|
|
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NM_000227.5:c.1802A>C
|
NP_000218.3:p.Glu601Ala
|
|
NM_001127717.3:c.6461A>C
|
NP_001121189.2:p.Glu2154Ala
|
|
NM_001127718.3:c.1634A>C
|
NP_001121190.2:p.Glu545Ala
|
|
NM_198129.3:c.6629A>C
|
NP_937762.2:p.Glu2210Ala
|
|
NM_000227.6:c.1802A>C
MANE Plus Clinical
|
NP_000218.3:p.Glu601Ala
|
|
NM_001127717.4:c.6461A>C
|
NP_001121189.2:p.Glu2154Ala
|
|
NM_001127718.4:c.1634A>C
|
NP_001121190.2:p.Glu545Ala
|
|
NM_198129.4:c.6629A>C
MANE Select
|
NP_937762.2:p.Glu2210Ala
|
|