ENST00000333868.10:c.441A>T
MANE Select
|
ENSP00000330237.5:p.Gly147=
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ENST00000333868.9:c.441A>T
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ENSP00000330237.5:p.Gly147=
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|
ENST00000348549.9:c.418+10225A>T
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ENSP00000255256.7:n.418+10225A>T
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ENST00000375890.8:c.192A>T
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ENSP00000365051.4:p.Gly64=
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ENST00000400777.7:c.433A>T
|
|
|
ENST00000440484.1:c.441A>T
|
ENSP00000411304.1:p.Gly147=
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|
ENST00000447522.5:c.192A>T
|
ENSP00000396540.1:p.Gly64=
|
|
ENST00000474305.2:c.301A>T
|
ENSP00000449216.1:n.301A>T
|
|
ENST00000546424.5:c.441A>T
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ENSP00000449584.1:p.Gly147=
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|
ENST00000546969.1:n.456A>T
|
|
|
NM_001229.4:c.441A>T
|
NP_001220.2:p.Gly147=
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|
NM_001278054.1:c.418+10225A>T
|
NP_001264983.1:n.418+10225A>T
|
|
NM_032996.3:c.192A>T
|
NP_127463.2:p.Gly64=
|
|
NR_102732.1:n.686A>T
|
|
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NR_102733.1:n.546A>T
|
|
|
XM_005246014.2:c.192A>T
|
XP_005246071.1:p.Gly64=
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|
XM_011542270.1:c.441A>T
|
XP_011540572.1:p.Gly147=
|
|
XM_011542271.1:c.192A>T
|
XP_011540573.1:p.Gly64=
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|
XM_011542272.1:c.192A>T
|
XP_011540574.1:p.Gly64=
|
|
XM_011542273.1:c.441A>T
|
XP_011540575.1:p.Gly147=
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|
XR_946778.1:n.606A>T
|
|
|
XM_011542273.3:c.441A>T
|
XP_011540575.1:p.Gly147=
|
|
NM_001229.5:c.441A>T
MANE Select
|
NP_001220.2:p.Gly147=
|
|
NM_001278054.2:c.418+10225A>T
|
NP_001264983.1:n.418+10225A>T
|
|
NR_102732.2:n.456A>T
|
|
|
NR_102733.2:n.316A>T
|
|
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