ENST00000402696.9:c.2000A>C
MANE Select
|
ENSP00000385834.3:p.Glu667Ala
|
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ENST00000402696.7:c.2000A>C
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ENSP00000385834.3:p.Glu667Ala
|
|
ENST00000461695.1:c.731A>C
|
|
|
ENST00000467842.1:n.2994A>C
|
|
|
NM_001063.3:c.2000A>C
|
NP_001054.1:p.Glu667Ala
|
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XM_011513100.1:c.2000A>C
|
XP_011511402.1:p.Glu667Ala
|
|
NM_001354703.1:c.1868A>C
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NP_001341632.1:p.Glu623Ala
|
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NM_001354704.1:c.1619A>C
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NP_001341633.1:p.Glu540Ala
|
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NM_001063.4:c.2000A>C
MANE Select
|
NP_001054.2:p.Glu667Ala
|
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NM_001354703.2:c.1868A>C
|
NP_001341632.2:p.Glu623Ala
|
|
NM_001354704.2:c.1619A>C
|
NP_001341633.2:p.Glu540Ala
|
|