ENST00000478003.2:n.2170A>C
|
|
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ENST00000682276.1:n.1787A>C
|
|
|
ENST00000682892.1:c.1889A>C
|
ENSP00000507214.1:p.Glu630Ala
|
|
ENST00000682952.1:n.1981A>C
|
|
|
ENST00000684455.1:c.1555A>C
|
|
|
ENST00000684642.1:c.1739A>C
|
ENSP00000507355.1:p.Glu580Ala
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|
ENST00000684740.1:n.2520A>C
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|
|
ENST00000303236.9:c.2342A>C
MANE Select
|
ENSP00000307235.3:p.Glu781Ala
|
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ENST00000652099.1:c.2536A>C
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|
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ENST00000652736.1:n.2218A>C
|
|
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ENST00000303236.7:c.2342A>C
|
ENSP00000307235.3:p.Glu781Ala
|
|
ENST00000415570.1:c.1979A>C
|
ENSP00000412076.1:p.Glu660Ala
|
|
ENST00000419748.5:c.1889A>C
|
ENSP00000408325.1:p.Glu630Ala
|
|
ENST00000470706.1:n.49-64A>C
|
|
|
NM_001313915.1:c.1889A>C
|
NP_001300844.1:p.Glu630Ala
|
|
NM_004836.5:c.2342A>C
|
NP_004827.4:p.Glu781Ala
|
|
NM_004836.6:c.2342A>C
|
NP_004827.4:p.Glu781Ala
|
|
NR_110236.1:n.1278T>G
|
|
|
XM_005264649.3:c.1658A>C
|
XP_005264706.1:p.Glu553Ala
|
|
XM_017005376.2:c.1658A>C
|
XP_016860865.1:p.Glu553Ala
|
|
NM_004836.7:c.2342A>C
MANE Select
|
NP_004827.4:p.Glu781Ala
|
|
NM_001313915.2:c.1889A>C
|
NP_001300844.1:p.Glu630Ala
|
|