ENST00000261208.8:c.1299C>G
MANE Select
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ENSP00000261208.3:p.Ala433=
|
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ENST00000261208.7:c.1299C>G
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ENSP00000261208.3:p.Ala433=
|
|
ENST00000538703.5:c.1299C>G
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ENSP00000440861.1:p.Ala433=
|
|
ENST00000541929.5:c.675C>G
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ENSP00000446364.1:p.Ala225=
|
|
ENST00000544080.6:c.*728C>G
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ENSP00000439385.2:n.*728C>G
|
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ENST00000546999.5:c.*728C>G
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ENSP00000447675.1:n.*728C>G
|
|
NM_001258333.1:c.675C>G
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NP_001245262.1:p.Ala225=
|
|
NM_001258334.1:c.1299C>G
|
NP_001245263.1:p.Ala433=
|
|
NM_002108.3:c.1299C>G
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NP_002099.1:p.Ala433=
|
|
XM_011538249.1:c.447C>G
|
XP_011536551.1:p.Ala149=
|
|
XM_011538249.2:c.447C>G
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XP_011536551.1:p.Ala149=
|
|
XM_017019246.1:c.369C>G
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XP_016874735.1:p.Ala123=
|
|
NM_002108.4:c.1299C>G
MANE Select
|
NP_002099.1:p.Ala433=
|
|
NM_001258334.2:c.1299C>G
|
NP_001245263.1:p.Ala433=
|
|
NM_001258333.2:c.675C>G
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NP_001245262.1:p.Ala225=
|
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