ENST00000380044.6:c.145G>C
MANE Select
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ENSP00000369383.1:p.Gly49Arg
|
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ENST00000233545.6:c.145G>C
|
ENSP00000233545.2:p.Gly49Arg
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ENST00000357186.10:c.19-263G>C
|
ENSP00000349713.6:n.19-263G>C
|
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ENST00000380044.5:c.145G>C
|
ENSP00000369383.1:p.Gly49Arg
|
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ENST00000402310.5:c.145G>C
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ENSP00000383955.1:p.Gly49Arg
|
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ENST00000402722.5:c.110G>C
|
ENSP00000386000.1:p.Arg37Thr
|
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ENST00000403262.6:c.145G>C
|
ENSP00000385671.1:p.Gly49Arg
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ENST00000405076.5:c.145G>C
|
ENSP00000385175.1:p.Gly49Arg
|
|
ENST00000405983.5:c.190G>C
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ENSP00000384586.1:p.Gly64Arg
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ENST00000415514.5:c.228-263G>C
|
ENSP00000388043.1:n.228-263G>C
|
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ENST00000426513.6:c.110G>C
|
ENSP00000403824.2:p.Arg37Thr
|
|
ENST00000428910.5:c.67G>C
|
ENSP00000405235.1:p.Gly23Arg
|
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ENST00000430991.5:c.75G>C
|
|
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ENST00000616446.1:n.122G>C
|
|
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ENST00000616707.1:n.353G>C
|
|
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ENST00000617583.4:n.171G>C
|
|
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ENST00000621183.4:n.201G>C
|
|
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ENST00000621470.4:n.161G>C
|
|
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ENST00000622003.4:n.318G>C
|
|
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NM_002437.4:c.145G>C
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NP_002428.1:p.Gly49Arg
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XM_005264326.2:c.145G>C
|
XP_005264383.1:p.Gly49Arg
|
|
XM_005264327.2:c.-15G>C
|
XP_005264384.1:n.-15G>C
|
|
XM_006712021.2:c.97G>C
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XP_006712084.1:p.Gly33Arg
|
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XM_005264326.4:c.145G>C
|
XP_005264383.1:p.Gly49Arg
|
|
XM_006712021.3:c.97G>C
|
XP_006712084.1:p.Gly33Arg
|
|
XM_017004150.1:c.127G>C
|
XP_016859639.1:p.Gly43Arg
|
|
XM_017004151.1:c.97G>C
|
XP_016859640.1:p.Gly33Arg
|
|
XM_017004152.1:c.-15G>C
|
XP_016859641.1:n.-15G>C
|
|
XM_024452913.1:c.97G>C
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XP_024308681.1:p.Gly33Arg
|
|
NM_002437.5:c.145G>C
MANE Select
|
NP_002428.1:p.Gly49Arg
|
|