ENST00000405460.9:c.14384G>A
MANE Select
|
ENSP00000384582.2:p.Gly4795Glu
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ENST00000425867.3:c.3338G>A
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ENSP00000392618.3:p.Gly1113Glu
|
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ENST00000507314.2:c.59G>A
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ENSP00000491299.1:p.Gly20Glu
|
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ENST00000638510.1:n.1651G>A
|
|
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ENST00000638585.1:n.150G>A
|
|
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ENST00000638975.1:c.1013G>A
|
ENSP00000492630.1:p.Gly338Glu
|
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ENST00000639431.1:c.265+115004G>A
|
ENSP00000491057.1:n.265+115004G>A
|
|
ENST00000640407.1:c.794G>A
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ENSP00000491425.1:p.Gly265Glu
|
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ENST00000405460.6:c.14384G>A
|
ENSP00000384582.2:p.Gly4795Glu
|
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ENST00000425867.2:c.1367G>A
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ENSP00000392618.2:p.Gly456Glu
|
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ENST00000507314.1:n.59G>A
|
|
|
NM_032119.3:c.14384G>A
|
NP_115495.3:p.Gly4795Glu
|
|
NR_003149.1:n.14397G>A
|
|
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XM_011543675.1:c.14381G>A
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XP_011541977.1:p.Gly4794Glu
|
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XM_011543676.1:c.14303G>A
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XP_011541978.1:p.Gly4768Glu
|
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XM_011543677.1:c.11687G>A
|
XP_011541979.1:p.Gly3896Glu
|
|
XM_011543678.1:c.14384G>A
|
XP_011541980.1:p.Gly4795Glu
|
|
NM_032119.4:c.14384G>A
MANE Select
|
NP_115495.3:p.Gly4795Glu
|
|
XM_017009963.2:c.14405G>A
|
XP_016865452.1:p.Gly4802Glu
|
|
XM_017009964.2:c.14402G>A
|
XP_016865453.1:p.Gly4801Glu
|
|
XM_017009965.1:c.14402G>A
|
XP_016865454.1:p.Gly4801Glu
|
|
XM_017009966.2:c.14324G>A
|
XP_016865455.1:p.Gly4775Glu
|
|
XM_017009967.1:c.14309G>A
|
XP_016865456.1:p.Gly4770Glu
|
|
XM_017009968.2:c.14405G>A
|
XP_016865457.1:p.Gly4802Glu
|
|
XM_017009969.2:c.14405G>A
|
XP_016865458.1:p.Gly4802Glu
|
|
XM_017009970.2:c.14405G>A
|
XP_016865459.1:p.Gly4802Glu
|
|
XM_017009971.2:c.14405G>A
|
XP_016865460.1:p.Gly4802Glu
|
|
XM_017009972.1:c.7523G>A
|
XP_016865461.1:p.Gly2508Glu
|
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XM_017009973.1:c.7502G>A
|
XP_016865462.1:p.Gly2501Glu
|
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NR_003149.2:n.14400G>A
|
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