ENST00000339818.9:c.272T>C
MANE Select
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ENSP00000344566.4:p.Val91Ala
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ENST00000325223.7:c.272T>C
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ENSP00000317302.7:p.Val91Ala
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ENST00000339818.8:c.272T>C
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ENSP00000344566.4:p.Val91Ala
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ENST00000397956.7:c.272T>C
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ENSP00000381047.3:p.Val91Ala
|
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ENST00000462742.1:n.2443T>C
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|
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ENST00000478674.1:n.331T>C
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|
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ENST00000496321.5:n.388T>C
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|
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NM_001271440.1:c.272T>C
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NP_001258369.1:p.Val91Ala
|
|
NM_001271441.1:c.272T>C
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NP_001258370.1:p.Val91Ala
|
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NM_001271442.1:c.149T>C
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NP_001258371.1:p.Val50Ala
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NM_004928.2:c.272T>C
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NP_004919.1:p.Val91Ala
|
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XM_006724051.2:c.347T>C
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XP_006724114.1:p.Val116Ala
|
|
XM_006724052.2:c.347T>C
|
XP_006724115.1:p.Val116Ala
|
|
XM_006724053.2:c.-53T>C
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XP_006724116.1:n.-53T>C
|
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XR_937571.1:n.475T>C
|
|
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XM_006724051.3:c.347T>C
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XP_006724114.1:p.Val116Ala
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|
XM_006724053.3:c.-53T>C
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XP_006724116.1:n.-53T>C
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|
XM_017028470.1:c.476T>C
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XP_016883959.1:p.Val159Ala
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|
XM_017028471.1:c.221T>C
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XP_016883960.1:p.Val74Ala
|
|
XM_017028472.1:c.-53T>C
|
XP_016883961.1:n.-53T>C
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XR_937571.2:n.482T>C
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|
|
NM_004928.3:c.272T>C
MANE Select
|
NP_004919.1:p.Val91Ala
|
|
NM_001271440.2:c.272T>C
|
NP_001258369.1:p.Val91Ala
|
|
NM_001271441.2:c.272T>C
|
NP_001258370.1:p.Val91Ala
|
|