ENST00000265631.10:c.891A>C
MANE Select
|
ENSP00000265631.6:p.Glu297Asp
|
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ENST00000265631.9:c.891A>C
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ENSP00000265631.5:p.Glu297Asp
|
|
ENST00000416240.6:c.891A>C
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ENSP00000400101.2:p.Glu297Asp
|
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ENST00000484495.5:n.44A>C
|
|
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NM_001160210.1:c.891A>C
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NP_001153682.1:p.Glu297Asp
|
|
NM_014251.2:c.891A>C
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NP_055066.1:p.Glu297Asp
|
|
NR_027662.1:n.966A>C
|
|
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XM_006715831.2:c.924A>C
|
XP_006715894.1:p.Glu308Asp
|
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XM_011515727.1:c.924A>C
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XP_011514029.1:p.Glu308Asp
|
|
XM_011515728.1:c.39A>C
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XP_011514030.1:p.Glu13Asp
|
|
XM_006715831.4:c.924A>C
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XP_006715894.1:p.Glu308Asp
|
|
XM_011515727.3:c.924A>C
|
XP_011514029.1:p.Glu308Asp
|
|
XM_017011663.1:c.882A>C
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XP_016867152.1:p.Glu294Asp
|
|
XM_017011664.2:c.39A>C
|
XP_016867153.1:p.Glu13Asp
|
|
XM_017011665.1:c.39A>C
|
XP_016867154.1:p.Glu13Asp
|
|
XR_001744525.2:n.1062A>C
|
|
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XR_002956405.1:n.1204A>C
|
|
|
NM_014251.3:c.891A>C
MANE Select
|
NP_055066.1:p.Glu297Asp
|
|
NR_027662.2:n.917A>C
|
|
|
NM_001160210.2:c.891A>C
|
NP_001153682.1:p.Glu297Asp
|
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