ENST00000380044.6:c.115G>C
MANE Select
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ENSP00000369383.1:p.Glu39Gln
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ENST00000233545.6:c.115G>C
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ENSP00000233545.2:p.Glu39Gln
|
|
ENST00000357186.10:c.19-293G>C
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ENSP00000349713.6:n.19-293G>C
|
|
ENST00000380044.5:c.115G>C
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ENSP00000369383.1:p.Glu39Gln
|
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ENST00000402310.5:c.115G>C
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ENSP00000383955.1:p.Glu39Gln
|
|
ENST00000402722.5:c.80G>C
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ENSP00000386000.1:p.Gly27Ala
|
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ENST00000403262.6:c.115G>C
|
ENSP00000385671.1:p.Glu39Gln
|
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ENST00000405076.5:c.115G>C
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ENSP00000385175.1:p.Glu39Gln
|
|
ENST00000405983.5:c.160G>C
|
ENSP00000384586.1:p.Glu54Gln
|
|
ENST00000415514.5:c.228-293G>C
|
ENSP00000388043.1:n.228-293G>C
|
|
ENST00000426513.6:c.80G>C
|
ENSP00000403824.2:p.Gly27Ala
|
|
ENST00000428910.5:c.37G>C
|
ENSP00000405235.1:p.Glu13Gln
|
|
ENST00000430991.5:c.45G>C
|
|
|
ENST00000616446.1:n.92G>C
|
|
|
ENST00000616707.1:n.323G>C
|
|
|
ENST00000617583.4:n.141G>C
|
|
|
ENST00000621183.4:n.171G>C
|
|
|
ENST00000621470.4:n.131G>C
|
|
|
ENST00000622003.4:n.288G>C
|
|
|
NM_002437.4:c.115G>C
|
NP_002428.1:p.Glu39Gln
|
|
XM_005264326.2:c.115G>C
|
XP_005264383.1:p.Glu39Gln
|
|
XM_005264327.2:c.-45G>C
|
XP_005264384.1:n.-45G>C
|
|
XM_006712021.2:c.67G>C
|
XP_006712084.1:p.Glu23Gln
|
|
XM_005264326.4:c.115G>C
|
XP_005264383.1:p.Glu39Gln
|
|
XM_006712021.3:c.67G>C
|
XP_006712084.1:p.Glu23Gln
|
|
XM_017004150.1:c.97G>C
|
XP_016859639.1:p.Glu33Gln
|
|
XM_017004151.1:c.67G>C
|
XP_016859640.1:p.Glu23Gln
|
|
XM_017004152.1:c.-45G>C
|
XP_016859641.1:n.-45G>C
|
|
XM_024452913.1:c.67G>C
|
XP_024308681.1:p.Glu23Gln
|
|
NM_002437.5:c.115G>C
MANE Select
|
NP_002428.1:p.Glu39Gln
|
|