ENST00000478003.2:n.2137A>C
|
|
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ENST00000682276.1:n.1754A>C
|
|
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ENST00000682892.1:c.1856A>C
|
ENSP00000507214.1:p.Asp619Ala
|
|
ENST00000682952.1:n.1948A>C
|
|
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ENST00000684455.1:c.1522A>C
|
|
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ENST00000684642.1:c.1706A>C
|
ENSP00000507355.1:p.Asp569Ala
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ENST00000684740.1:n.2487A>C
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|
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ENST00000303236.9:c.2309A>C
MANE Select
|
ENSP00000307235.3:p.Asp770Ala
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ENST00000652099.1:c.2503A>C
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|
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ENST00000652736.1:n.2185A>C
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|
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ENST00000303236.7:c.2309A>C
|
ENSP00000307235.3:p.Asp770Ala
|
|
ENST00000415570.1:c.1946A>C
|
ENSP00000412076.1:p.Asp649Ala
|
|
ENST00000419748.5:c.1856A>C
|
ENSP00000408325.1:p.Asp619Ala
|
|
ENST00000470706.1:n.49-97A>C
|
|
|
NM_001313915.1:c.1856A>C
|
NP_001300844.1:p.Asp619Ala
|
|
NM_004836.5:c.2309A>C
|
NP_004827.4:p.Asp770Ala
|
|
NM_004836.6:c.2309A>C
|
NP_004827.4:p.Asp770Ala
|
|
NR_110236.1:n.1311T>G
|
|
|
XM_005264649.3:c.1625A>C
|
XP_005264706.1:p.Asp542Ala
|
|
XM_017005376.2:c.1625A>C
|
XP_016860865.1:p.Asp542Ala
|
|
NM_004836.7:c.2309A>C
MANE Select
|
NP_004827.4:p.Asp770Ala
|
|
NM_001313915.2:c.1856A>C
|
NP_001300844.1:p.Asp619Ala
|
|