ENST00000478003.2:n.2200A>C
|
|
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ENST00000682276.1:n.1817A>C
|
|
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ENST00000682892.1:c.1919A>C
|
ENSP00000507214.1:p.Glu640Ala
|
|
ENST00000682952.1:n.2011A>C
|
|
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ENST00000684455.1:c.1585A>C
|
|
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ENST00000684642.1:c.1769A>C
|
ENSP00000507355.1:p.Glu590Ala
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ENST00000684740.1:n.2550A>C
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|
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ENST00000303236.9:c.2372A>C
MANE Select
|
ENSP00000307235.3:p.Glu791Ala
|
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ENST00000652099.1:c.2566A>C
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|
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ENST00000652736.1:n.2248A>C
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|
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ENST00000303236.7:c.2372A>C
|
ENSP00000307235.3:p.Glu791Ala
|
|
ENST00000415570.1:c.2009A>C
|
ENSP00000412076.1:p.Glu670Ala
|
|
ENST00000419748.5:c.1919A>C
|
ENSP00000408325.1:p.Glu640Ala
|
|
ENST00000470706.1:n.49-34A>C
|
|
|
NM_001313915.1:c.1919A>C
|
NP_001300844.1:p.Glu640Ala
|
|
NM_004836.5:c.2372A>C
|
NP_004827.4:p.Glu791Ala
|
|
NM_004836.6:c.2372A>C
|
NP_004827.4:p.Glu791Ala
|
|
NR_110236.1:n.1248T>G
|
|
|
XM_005264649.3:c.1688A>C
|
XP_005264706.1:p.Glu563Ala
|
|
XM_017005376.2:c.1688A>C
|
XP_016860865.1:p.Glu563Ala
|
|
NM_004836.7:c.2372A>C
MANE Select
|
NP_004827.4:p.Glu791Ala
|
|
NM_001313915.2:c.1919A>C
|
NP_001300844.1:p.Glu640Ala
|
|