ENST00000614565.5:c.1772G>C
MANE Select
|
ENSP00000484928.1:p.Gly591Ala
|
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ENST00000543233.2:c.1550G>C
|
ENSP00000443301.1:p.Gly517Ala
|
|
ENST00000611855.4:c.1490G>C
|
ENSP00000480844.1:p.Gly497Ala
|
|
ENST00000614565.4:c.1772G>C
|
ENSP00000484928.1:p.Gly591Ala
|
|
NM_001252338.2:c.1661G>C
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NP_001239267.1:p.Gly554Ala
|
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NM_001252339.2:c.1550G>C
|
NP_001239268.1:p.Gly517Ala
|
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NM_001794.4:c.1772G>C
|
NP_001785.2:p.Gly591Ala
|
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NM_001794.5:c.1772G>C
MANE Select
|
NP_001785.2:p.Gly591Ala
|
|
NM_001252339.3:c.1550G>C
|
NP_001239268.1:p.Gly517Ala
|
|