ENST00000265631.10:c.1784T>A
MANE Select
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ENSP00000265631.6:p.Val595Glu
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ENST00000265631.9:c.1784T>A
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ENSP00000265631.5:p.Val595Glu
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|
ENST00000416240.6:c.1787T>A
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ENSP00000400101.2:p.Val596Glu
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ENST00000494085.1:n.287T>A
|
|
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NM_001160210.1:c.1787T>A
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NP_001153682.1:p.Val596Glu
|
|
NM_014251.2:c.1784T>A
|
NP_055066.1:p.Val595Glu
|
|
NR_027662.1:n.1859T>A
|
|
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XM_006715831.2:c.1817T>A
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XP_006715894.1:p.Val606Glu
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XM_011515728.1:c.932T>A
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XP_011514030.1:p.Val311Glu
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XM_006715831.4:c.1817T>A
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XP_006715894.1:p.Val606Glu
|
|
XM_017011663.1:c.1775T>A
|
XP_016867152.1:p.Val592Glu
|
|
XM_017011664.2:c.932T>A
|
XP_016867153.1:p.Val311Glu
|
|
XM_017011665.1:c.932T>A
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XP_016867154.1:p.Val311Glu
|
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XR_001744525.2:n.2030T>A
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|
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XR_002956405.1:n.2588T>A
|
|
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NM_014251.3:c.1784T>A
MANE Select
|
NP_055066.1:p.Val595Glu
|
|
NR_027662.2:n.1810T>A
|
|
|
NM_001160210.2:c.1787T>A
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NP_001153682.1:p.Val596Glu
|
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