ENST00000261208.8:c.849T>A
MANE Select
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ENSP00000261208.3:p.Ala283=
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ENST00000261208.7:c.849T>A
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ENSP00000261208.3:p.Ala283=
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ENST00000538703.5:c.849T>A
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ENSP00000440861.1:p.Ala283=
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ENST00000541929.5:c.225T>A
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ENSP00000446364.1:p.Ala75=
|
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ENST00000544080.6:c.*278T>A
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ENSP00000439385.2:n.*278T>A
|
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ENST00000546999.5:c.*278T>A
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ENSP00000447675.1:n.*278T>A
|
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ENST00000549376.1:n.242T>A
|
|
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ENST00000551562.1:n.109T>A
|
|
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ENST00000552509.5:c.813T>A
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ENSP00000450372.1:p.Ala271=
|
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NM_001258333.1:c.225T>A
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NP_001245262.1:p.Ala75=
|
|
NM_001258334.1:c.849T>A
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NP_001245263.1:p.Ala283=
|
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NM_002108.3:c.849T>A
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NP_002099.1:p.Ala283=
|
|
XM_011538249.1:c.4-2159T>A
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XP_011536551.1:n.4-2159T>A
|
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XM_011538249.2:c.4-2159T>A
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XP_011536551.1:n.4-2159T>A
|
|
NM_002108.4:c.849T>A
MANE Select
|
NP_002099.1:p.Ala283=
|
|
NM_001258334.2:c.849T>A
|
NP_001245263.1:p.Ala283=
|
|
NM_001258333.2:c.225T>A
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NP_001245262.1:p.Ala75=
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