ENST00000265631.10:c.873A>C
MANE Select
|
ENSP00000265631.6:p.Glu291Asp
|
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ENST00000265631.9:c.873A>C
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ENSP00000265631.5:p.Glu291Asp
|
|
ENST00000416240.6:c.873A>C
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ENSP00000400101.2:p.Glu291Asp
|
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ENST00000484495.5:n.26A>C
|
|
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NM_001160210.1:c.873A>C
|
NP_001153682.1:p.Glu291Asp
|
|
NM_014251.2:c.873A>C
|
NP_055066.1:p.Glu291Asp
|
|
NR_027662.1:n.948A>C
|
|
|
XM_006715831.2:c.906A>C
|
XP_006715894.1:p.Glu302Asp
|
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XM_011515727.1:c.906A>C
|
XP_011514029.1:p.Glu302Asp
|
|
XM_011515728.1:c.21A>C
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XP_011514030.1:p.Glu7Asp
|
|
XM_006715831.4:c.906A>C
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XP_006715894.1:p.Glu302Asp
|
|
XM_011515727.3:c.906A>C
|
XP_011514029.1:p.Glu302Asp
|
|
XM_017011663.1:c.864A>C
|
XP_016867152.1:p.Glu288Asp
|
|
XM_017011664.2:c.21A>C
|
XP_016867153.1:p.Glu7Asp
|
|
XM_017011665.1:c.21A>C
|
XP_016867154.1:p.Glu7Asp
|
|
XR_001744525.2:n.1044A>C
|
|
|
XR_002956405.1:n.1186A>C
|
|
|
NM_014251.3:c.873A>C
MANE Select
|
NP_055066.1:p.Glu291Asp
|
|
NR_027662.2:n.899A>C
|
|
|
NM_001160210.2:c.873A>C
|
NP_001153682.1:p.Glu291Asp
|
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