ENST00000262367.10:c.6292G>A
MANE Select
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ENSP00000262367.5:p.Ala2098Thr
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ENST00000262367.9:c.6292G>A
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ENSP00000262367.5:p.Ala2098Thr
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ENST00000382070.7:c.6178G>A
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ENSP00000371502.3:p.Ala2060Thr
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NM_001079846.1:c.6178G>A
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NP_001073315.1:p.Ala2060Thr
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NM_004380.2:c.6292G>A
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NP_004371.2:p.Ala2098Thr
|
|
XM_005255124.3:c.6247G>A
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XP_005255181.1:p.Ala2083Thr
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XM_005255125.3:c.5875G>A
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XP_005255182.1:p.Ala1959Thr
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XM_006720848.2:c.6031G>A
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XP_006720911.1:p.Ala2011Thr
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XM_011522380.1:c.6238G>A
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XP_011520682.1:p.Ala2080Thr
|
|
XM_011522381.1:c.5539G>A
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XP_011520683.1:p.Ala1847Thr
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XM_005255124.4:c.6247G>A
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XP_005255181.1:p.Ala2083Thr
|
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XM_005255125.4:c.5875G>A
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XP_005255182.1:p.Ala1959Thr
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XM_006720848.3:c.6031G>A
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XP_006720911.1:p.Ala2011Thr
|
|
XM_011522381.2:c.5539G>A
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XP_011520683.1:p.Ala1847Thr
|
|
XM_017022944.1:c.6286G>A
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XP_016878433.1:p.Ala2096Thr
|
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NM_004380.3:c.6292G>A
MANE Select
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NP_004371.2:p.Ala2098Thr
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