ENST00000478003.2:n.2032A>C
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ENST00000682276.1:n.1649A>C
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ENST00000682892.1:c.1751A>C
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ENSP00000507214.1:p.Glu584Ala
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ENST00000682952.1:n.1843A>C
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ENST00000684455.1:c.1417A>C
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ENST00000684642.1:c.1601A>C
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ENSP00000507355.1:p.Glu534Ala
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ENST00000684740.1:n.2382A>C
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ENST00000303236.9:c.2204A>C
MANE Select
|
ENSP00000307235.3:p.Glu735Ala
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ENST00000652099.1:c.2398A>C
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ENST00000652736.1:n.2080A>C
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ENST00000303236.7:c.2204A>C
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ENSP00000307235.3:p.Glu735Ala
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|
ENST00000415570.1:c.1841A>C
|
ENSP00000412076.1:p.Glu614Ala
|
|
ENST00000419748.5:c.1751A>C
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ENSP00000408325.1:p.Glu584Ala
|
|
ENST00000470706.1:n.48+82A>C
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|
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NM_001313915.1:c.1751A>C
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NP_001300844.1:p.Glu584Ala
|
|
NM_004836.5:c.2204A>C
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NP_004827.4:p.Glu735Ala
|
|
NM_004836.6:c.2204A>C
|
NP_004827.4:p.Glu735Ala
|
|
NR_110236.1:n.1416T>G
|
|
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XM_005264649.3:c.1520A>C
|
XP_005264706.1:p.Glu507Ala
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XR_939749.1:n.2483A>C
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|
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XM_017005376.2:c.1520A>C
|
XP_016860865.1:p.Glu507Ala
|
|
NM_004836.7:c.2204A>C
MANE Select
|
NP_004827.4:p.Glu735Ala
|
|
NM_001313915.2:c.1751A>C
|
NP_001300844.1:p.Glu584Ala
|
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