ENST00000296051.7:c.1127C>A
MANE Select
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ENSP00000296051.2:p.Ala376Glu
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ENST00000296051.6:c.1127C>A
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ENSP00000296051.2:p.Ala376Glu
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ENST00000460120.5:c.632C>A
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ENSP00000418230.1:p.Ala211Glu
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ENST00000462030.5:n.1726C>A
|
|
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ENST00000486530.1:n.1160C>A
|
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NM_001308258.1:c.632C>A
|
NP_001295187.1:p.Ala211Glu
|
|
NM_032383.3:c.1127C>A
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NP_115759.2:p.Ala376Glu
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NM_032383.4:c.1127C>A
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NP_115759.2:p.Ala376Glu
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XM_005247834.3:c.1127C>A
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XP_005247891.1:p.Ala376Glu
|
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XM_006713788.1:c.1127C>A
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XP_006713851.1:p.Ala376Glu
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XR_924201.1:n.1242C>A
|
|
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XM_005247834.4:c.1127C>A
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XP_005247891.1:p.Ala376Glu
|
|
XM_017007323.2:c.1127C>A
|
XP_016862812.1:p.Ala376Glu
|
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XR_001740326.2:n.1227C>A
|
|
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XR_001740327.2:n.1227C>A
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XR_001740328.2:n.1227C>A
|
|
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XR_924201.3:n.1227C>A
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|
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NM_001308258.2:c.632C>A
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NP_001295187.1:p.Ala211Glu
|
|
NM_032383.5:c.1127C>A
MANE Select
|
NP_115759.2:p.Ala376Glu
|
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