ENST00000402696.9:c.1688G>C
MANE Select
|
ENSP00000385834.3:p.Gly563Ala
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ENST00000402696.7:c.1688G>C
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ENSP00000385834.3:p.Gly563Ala
|
|
ENST00000461695.1:c.419G>C
|
|
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ENST00000467842.1:n.2682G>C
|
|
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NM_001063.3:c.1688G>C
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NP_001054.1:p.Gly563Ala
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XM_011513100.1:c.1688G>C
|
XP_011511402.1:p.Gly563Ala
|
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NM_001354703.1:c.1556G>C
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NP_001341632.1:p.Gly519Ala
|
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NM_001354704.1:c.1307G>C
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NP_001341633.1:p.Gly436Ala
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NM_001063.4:c.1688G>C
MANE Select
|
NP_001054.2:p.Gly563Ala
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NM_001354703.2:c.1556G>C
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NP_001341632.2:p.Gly519Ala
|
|
NM_001354704.2:c.1307G>C
|
NP_001341633.2:p.Gly436Ala
|
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