ENST00000242317.9:c.1821C>A
MANE Select
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ENSP00000242317.4:p.Ala607=
|
|
ENST00000242317.8:c.1821C>A
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ENSP00000242317.4:p.Ala607=
|
|
ENST00000442556.1:c.329+2548C>A
|
|
|
ENST00000470169.5:c.609C>A
|
|
|
ENST00000485580.1:n.397C>A
|
|
|
ENST00000614641.4:c.1833C>A
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ENSP00000480538.1:p.Ala611=
|
|
NM_001281428.1:c.1833C>A
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NP_001268357.1:p.Ala611=
|
|
NM_012144.3:c.1821C>A
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NP_036276.1:p.Ala607=
|
|
XM_006716758.2:c.1290C>A
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XP_006716821.1:p.Ala430=
|
|
XM_011517848.1:c.1575C>A
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XP_011516150.1:p.Ala525=
|
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XM_006716758.3:c.1290C>A
|
XP_006716821.1:p.Ala430=
|
|
XM_011517848.2:c.1575C>A
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XP_011516150.1:p.Ala525=
|
|
XM_017014625.2:c.1563C>A
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XP_016870114.1:p.Ala521=
|
|
XR_002956774.1:n.1924C>A
|
|
|
NM_012144.4:c.1821C>A
MANE Select
|
NP_036276.1:p.Ala607=
|
|
NM_001281428.2:c.1833C>A
|
NP_001268357.1:p.Ala611=
|
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