ENST00000313468.10:c.165A>G
MANE Select
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ENSP00000315774.5:p.Ala55=
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ENST00000313468.9:c.165A>G
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ENSP00000315774.5:p.Ala55=
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ENST00000432321.6:n.282A>G
|
|
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ENST00000453471.6:c.165A>G
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ENSP00000403972.2:p.Ala55=
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ENST00000525419.5:c.111A>G
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ENSP00000433521.1:p.Ala37=
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ENST00000525628.1:c.165A>G
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ENSP00000432968.1:p.Ala55=
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|
ENST00000526339.5:c.165A>G
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ENSP00000436287.1:p.Ala55=
|
|
ENST00000526446.5:c.*220A>G
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ENSP00000433645.1:n.*220A>G
|
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ENST00000528492.1:c.-67+2245A>G
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ENSP00000432848.1:n.-67+2245A>G
|
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ENST00000529645.1:c.343A>G
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ENSP00000431293.1:n.343A>G
|
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ENST00000531228.1:c.*7A>G
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ENSP00000433054.1:n.*7A>G
|
|
ENST00000532399.1:n.772A>G
|
|
|
NM_002496.3:c.165A>G
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NP_002487.1:p.Ala55=
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XM_005274013.1:c.165A>G
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XP_005274070.1:p.Ala55=
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|
XM_005274014.1:c.165A>G
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XP_005274071.1:p.Ala55=
|
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XM_005274015.1:c.45A>G
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XP_005274072.1:p.Ala15=
|
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XM_011545053.1:c.165A>G
|
XP_011543355.1:p.Ala55=
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|
NM_002496.4:c.165A>G
MANE Select
|
NP_002487.1:p.Ala55=
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