ENST00000261819.8:c.1706T>C
MANE Select
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ENSP00000261819.3:p.Val569Ala
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ENST00000261819.7:c.1706T>C
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ENSP00000261819.3:p.Val569Ala
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ENST00000366333.3:n.918T>C
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ENST00000441917.6:c.1370T>C
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ENSP00000415061.2:p.Val457Ala
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ENST00000534976.5:n.2362T>C
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ENST00000535482.1:c.704T>C
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ENSP00000438754.1:p.Val235Ala
|
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ENST00000535641.5:n.1917T>C
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|
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ENST00000539079.5:c.1050T>C
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|
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ENST00000541887.5:c.1667T>C
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ENSP00000439875.1:p.Val556Ala
|
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ENST00000544314.5:n.824T>C
|
|
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ENST00000545218.5:n.949T>C
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|
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NM_001137559.1:c.1370T>C
|
NP_001131031.1:p.Val457Ala
|
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NM_016237.4:c.1706T>C
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NP_057321.2:p.Val569Ala
|
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XM_005253900.2:c.1667T>C
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XP_005253957.1:p.Val556Ala
|
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XM_006719449.1:c.512T>C
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XP_006719512.1:p.Val171Ala
|
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NM_001330489.1:c.1667T>C
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NP_001317418.1:p.Val556Ala
|
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XM_017019423.2:c.512T>C
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XP_016874912.1:p.Val171Ala
|
|
XM_017019424.2:c.512T>C
|
XP_016874913.1:p.Val171Ala
|
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NM_016237.5:c.1706T>C
MANE Select
|
NP_057321.2:p.Val569Ala
|
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NM_001330489.2:c.1667T>C
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NP_001317418.1:p.Val556Ala
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