ENST00000248633.9:c.2757A>G
MANE Select
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ENSP00000248633.4:p.Glu919=
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ENST00000248633.8:c.2757A>G
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ENSP00000248633.4:p.Glu919=
|
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ENST00000428214.5:c.2586A>G
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ENSP00000394413.1:p.Glu862=
|
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ENST00000438045.5:c.1791A>G
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ENSP00000410438.1:p.Glu597=
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ENST00000484913.5:n.2796A>G
|
|
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ENST00000496420.5:n.2649A>G
|
|
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NM_000466.2:c.2757A>G
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NP_000457.1:p.Glu919=
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NM_001282677.1:c.2586A>G
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NP_001269606.1:p.Glu862=
|
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NM_001282678.1:c.2133A>G
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NP_001269607.1:p.Glu711=
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XM_005250433.3:c.1008A>G
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XP_005250490.1:p.Glu336=
|
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XR_242246.3:n.2853A>G
|
|
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XM_017012319.2:c.1008A>G
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XP_016867808.1:p.Glu336=
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XR_001744808.2:n.1784A>G
|
|
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XR_242246.5:n.2804A>G
|
|
|
NM_000466.3:c.2757A>G
MANE Select
|
NP_000457.1:p.Glu919=
|
|
NM_001282677.2:c.2586A>G
|
NP_001269606.1:p.Glu862=
|
|
NM_001282678.2:c.2133A>G
|
NP_001269607.1:p.Glu711=
|
|