ENST00000426333.7:c.2103G>A
MANE Select
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ENSP00000392094.1:p.Glu701=
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ENST00000402521.7:c.1998G>A
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ENSP00000385873.2:p.Glu666=
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ENST00000426333.6:c.2103G>A
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ENSP00000392094.1:p.Glu701=
|
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ENST00000586276.5:n.1765G>A
|
|
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ENST00000590124.5:c.105G>A
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ENSP00000467249.1:p.Glu35=
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ENST00000590367.5:n.1831G>A
|
|
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ENST00000590977.5:n.711G>A
|
|
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ENST00000591382.5:c.2103G>A
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ENSP00000467805.1:p.Glu701=
|
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ENST00000592576.5:c.2073G>A
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ENSP00000465058.1:p.Glu691=
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NM_001142605.1:c.1998G>A
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NP_001136077.1:p.Glu666=
|
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NM_001258353.1:c.2103G>A
|
NP_001245282.1:p.Glu701=
|
|
NM_001258354.1:c.2073G>A
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NP_001245283.1:p.Glu691=
|
|
NM_004247.3:c.2103G>A
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NP_004238.3:p.Glu701=
|
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XR_934602.1:n.2188G>A
|
|
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XR_934602.3:n.2184G>A
|
|
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NM_004247.4:c.2103G>A
MANE Select
|
NP_004238.3:p.Glu701=
|
|
NM_001142605.2:c.1998G>A
|
NP_001136077.1:p.Glu666=
|
|
NM_001258353.2:c.2103G>A
|
NP_001245282.1:p.Glu701=
|
|
NM_001258354.2:c.2073G>A
|
NP_001245283.1:p.Glu691=
|
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