ENST00000267845.8:c.1782T>G
MANE Select
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ENSP00000267845.3:p.Ala594=
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ENST00000267845.7:c.1782T>G
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ENSP00000267845.3:p.Ala594=
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ENST00000543581.5:c.1683T>G
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ENSP00000440252.1:p.Ala561=
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ENST00000559816.1:n.1526T>G
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|
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NM_001306146.1:c.1683T>G
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NP_001293075.1:p.Ala561=
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NM_002112.3:c.1782T>G
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NP_002103.2:p.Ala594=
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XM_011521479.1:c.1545T>G
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XP_011519781.1:p.Ala515=
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XM_011521480.1:c.1350T>G
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XP_011519782.1:p.Ala450=
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XM_017022094.1:c.1887T>G
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XP_016877583.1:p.Ala629=
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XM_017022095.1:c.1788T>G
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XP_016877584.1:p.Ala596=
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XM_017022096.1:c.1659T>G
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XP_016877585.1:p.Ala553=
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XM_017022097.1:c.1650T>G
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XP_016877586.1:p.Ala550=
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XM_017022098.1:c.1455T>G
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XP_016877587.1:p.Ala485=
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NM_002112.4:c.1782T>G
MANE Select
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NP_002103.2:p.Ala594=
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NM_001306146.2:c.1683T>G
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NP_001293075.1:p.Ala561=
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