ENST00000248633.9:c.2024A>C
MANE Select
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ENSP00000248633.4:p.Glu675Ala
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ENST00000248633.8:c.2024A>C
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ENSP00000248633.4:p.Glu675Ala
|
|
ENST00000428214.5:c.1900+1469A>C
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ENSP00000394413.1:n.1900+1469A>C
|
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ENST00000438045.5:c.1058A>C
|
ENSP00000410438.1:p.Glu353Ala
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ENST00000484913.5:n.2063A>C
|
|
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ENST00000496420.5:n.1700A>C
|
|
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NM_000466.2:c.2024A>C
|
NP_000457.1:p.Glu675Ala
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NM_001282677.1:c.1900+1469A>C
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NP_001269606.1:n.1900+1469A>C
|
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NM_001282678.1:c.1400A>C
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NP_001269607.1:p.Glu467Ala
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XM_005250433.3:c.275A>C
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XP_005250490.1:p.Glu92Ala
|
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XR_242246.3:n.2120A>C
|
|
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XM_017012319.2:c.275A>C
|
XP_016867808.1:p.Glu92Ala
|
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XR_001744808.2:n.1051A>C
|
|
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XR_242246.5:n.2071A>C
|
|
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NM_000466.3:c.2024A>C
MANE Select
|
NP_000457.1:p.Glu675Ala
|
|
NM_001282677.2:c.1900+1469A>C
|
NP_001269606.1:n.1900+1469A>C
|
|
NM_001282678.2:c.1400A>C
|
NP_001269607.1:p.Glu467Ala
|
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