ENST00000525748.6:c.1411G>A
MANE Select
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ENSP00000434364.2:p.Ala471Thr
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ENST00000298923.11:c.*708G>A
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ENSP00000298923.7:n.*708G>A
|
|
ENST00000525748.5:c.1411G>A
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ENSP00000434364.1:p.Ala471Thr
|
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NM_004211.3:c.1411G>A
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NP_004202.2:p.Ala471Thr
|
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XM_005253225.1:c.709G>A
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XP_005253282.1:p.Ala237Thr
|
|
XM_011520473.1:c.1411G>A
|
XP_011518775.1:p.Ala471Thr
|
|
NM_001318369.1:c.709G>A
|
NP_001305298.1:p.Ala237Thr
|
|
NM_004211.4:c.1411G>A
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NP_004202.3:p.Ala471Thr
|
|
XM_017018544.2:c.535G>A
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XP_016874033.1:p.Ala179Thr
|
|
XM_017018545.2:c.370G>A
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XP_016874034.1:p.Ala124Thr
|
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NM_001318369.2:c.709G>A
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NP_001305298.1:p.Ala237Thr
|
|
NM_004211.5:c.1411G>A
MANE Select
|
NP_004202.4:p.Ala471Thr
|
|