ENST00000370263.9:c.950T>C
MANE Select
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ENSP00000359285.4:p.Val317Ala
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ENST00000370263.8:c.950T>C
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ENSP00000359285.4:p.Val317Ala
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ENST00000463705.5:n.1598T>C
|
|
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ENST00000467563.3:n.1020T>C
|
|
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ENST00000498043.6:c.974T>C
|
|
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ENST00000615287.4:c.737T>C
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ENSP00000483388.1:p.Val246Ala
|
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ENST00000627000.1:c.*639T>C
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ENSP00000486914.1:n.*639T>C
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ENST00000630240.1:n.671T>C
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NM_000744.6:c.950T>C
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NP_000735.1:p.Val317Ala
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NM_001256573.1:c.422T>C
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NP_001243502.1:p.Val141Ala
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NR_046317.1:n.1206T>C
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|
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XM_011528524.1:c.737T>C
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XP_011526826.1:p.Val246Ala
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XM_017027625.2:c.422T>C
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XP_016883114.1:p.Val141Ala
|
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XM_024451822.1:c.422T>C
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XP_024307590.1:p.Val141Ala
|
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NM_001256573.2:c.422T>C
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NP_001243502.1:p.Val141Ala
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NR_046317.2:n.1159T>C
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|
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NM_000744.7:c.950T>C
MANE Select
|
NP_000735.1:p.Val317Ala
|
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