ENST00000405460.9:c.884G>A
MANE Select
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ENSP00000384582.2:p.Gly295Glu
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ENST00000640083.1:n.589G>A
|
|
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ENST00000640109.1:n.980G>A
|
|
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ENST00000640281.1:n.943G>A
|
|
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ENST00000405460.6:c.884G>A
|
ENSP00000384582.2:p.Gly295Glu
|
|
NM_032119.3:c.884G>A
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NP_115495.3:p.Gly295Glu
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NR_003149.1:n.980G>A
|
|
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XM_011543675.1:c.884G>A
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XP_011541977.1:p.Gly295Glu
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XM_011543676.1:c.884G>A
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XP_011541978.1:p.Gly295Glu
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XM_011543678.1:c.884G>A
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XP_011541980.1:p.Gly295Glu
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XM_011543679.1:c.884G>A
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XP_011541981.1:p.Gly295Glu
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|
NM_032119.4:c.884G>A
MANE Select
|
NP_115495.3:p.Gly295Glu
|
|
XM_017009963.2:c.884G>A
|
XP_016865452.1:p.Gly295Glu
|
|
XM_017009964.2:c.884G>A
|
XP_016865453.1:p.Gly295Glu
|
|
XM_017009965.1:c.881G>A
|
XP_016865454.1:p.Gly294Glu
|
|
XM_017009966.2:c.884G>A
|
XP_016865455.1:p.Gly295Glu
|
|
XM_017009967.1:c.788G>A
|
XP_016865456.1:p.Gly263Glu
|
|
XM_017009968.2:c.884G>A
|
XP_016865457.1:p.Gly295Glu
|
|
XM_017009969.2:c.884G>A
|
XP_016865458.1:p.Gly295Glu
|
|
XM_017009970.2:c.884G>A
|
XP_016865459.1:p.Gly295Glu
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|
XM_017009971.2:c.884G>A
|
XP_016865460.1:p.Gly295Glu
|
|
XM_017009974.2:c.884G>A
|
XP_016865463.1:p.Gly295Glu
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NR_003149.2:n.983G>A
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