ENST00000242317.9:c.263A>C
MANE Select
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ENSP00000242317.4:p.Glu88Ala
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ENST00000242317.8:c.263A>C
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ENSP00000242317.4:p.Glu88Ala
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ENST00000437363.5:c.230A>C
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ENSP00000395396.1:p.Glu77Ala
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ENST00000488369.1:n.379A>C
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ENST00000614641.4:c.263A>C
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ENSP00000480538.1:p.Glu88Ala
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NM_001281428.1:c.263A>C
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NP_001268357.1:p.Glu88Ala
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NM_012144.3:c.263A>C
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NP_036276.1:p.Glu88Ala
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XM_011517846.1:c.263A>C
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XP_011516148.1:p.Glu88Ala
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XM_011517847.1:c.263A>C
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XP_011516149.1:p.Glu88Ala
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XM_011517848.1:c.263A>C
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XP_011516150.1:p.Glu88Ala
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XM_011517849.1:c.263A>C
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XP_011516151.1:p.Glu88Ala
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XM_011517850.1:c.263A>C
|
XP_011516152.1:p.Glu88Ala
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XR_929232.1:n.517A>C
|
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XR_929233.1:n.517A>C
|
|
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XR_929235.1:n.517A>C
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XM_006716758.3:c.-214A>C
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XP_006716821.1:n.-214A>C
|
|
XM_011517846.2:c.263A>C
|
XP_011516148.1:p.Glu88Ala
|
|
XM_011517847.3:c.263A>C
|
XP_011516149.1:p.Glu88Ala
|
|
XM_011517848.2:c.263A>C
|
XP_011516150.1:p.Glu88Ala
|
|
XM_011517849.2:c.263A>C
|
XP_011516151.1:p.Glu88Ala
|
|
XM_011517850.3:c.263A>C
|
XP_011516152.1:p.Glu88Ala
|
|
XM_017014625.2:c.263A>C
|
XP_016870114.1:p.Glu88Ala
|
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XR_002956774.1:n.464A>C
|
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XR_929232.2:n.464A>C
|
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XR_929233.2:n.464A>C
|
|
|
NM_012144.4:c.263A>C
MANE Select
|
NP_036276.1:p.Glu88Ala
|
|
NM_001281428.2:c.263A>C
|
NP_001268357.1:p.Glu88Ala
|
|