ENST00000478003.2:n.2143A>C
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ENST00000682276.1:n.1760A>C
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ENST00000682892.1:c.1862A>C
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ENSP00000507214.1:p.Glu621Ala
|
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ENST00000682952.1:n.1954A>C
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ENST00000684455.1:c.1528A>C
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ENST00000684642.1:c.1712A>C
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ENSP00000507355.1:p.Glu571Ala
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ENST00000684740.1:n.2493A>C
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ENST00000303236.9:c.2315A>C
MANE Select
|
ENSP00000307235.3:p.Glu772Ala
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ENST00000652099.1:c.2509A>C
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ENST00000652736.1:n.2191A>C
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ENST00000303236.7:c.2315A>C
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ENSP00000307235.3:p.Glu772Ala
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ENST00000415570.1:c.1952A>C
|
ENSP00000412076.1:p.Glu651Ala
|
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ENST00000419748.5:c.1862A>C
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ENSP00000408325.1:p.Glu621Ala
|
|
ENST00000470706.1:n.49-91A>C
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|
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NM_001313915.1:c.1862A>C
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NP_001300844.1:p.Glu621Ala
|
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NM_004836.5:c.2315A>C
|
NP_004827.4:p.Glu772Ala
|
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NM_004836.6:c.2315A>C
|
NP_004827.4:p.Glu772Ala
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NR_110236.1:n.1305T>G
|
|
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XM_005264649.3:c.1631A>C
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XP_005264706.1:p.Glu544Ala
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|
XM_017005376.2:c.1631A>C
|
XP_016860865.1:p.Glu544Ala
|
|
NM_004836.7:c.2315A>C
MANE Select
|
NP_004827.4:p.Glu772Ala
|
|
NM_001313915.2:c.1862A>C
|
NP_001300844.1:p.Glu621Ala
|
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