ENST00000255078.8:c.2004A>T
MANE Select
|
ENSP00000255078.4:p.Gly668=
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ENST00000674675.1:c.248A>T
|
|
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ENST00000674878.1:c.248A>T
|
|
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ENST00000674955.1:c.*721A>T
|
ENSP00000502463.1:n.*721A>T
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ENST00000675118.1:c.1492A>T
|
|
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ENST00000675389.1:n.279A>T
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|
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ENST00000675615.1:c.2004A>T
|
ENSP00000502413.1:p.Gly668=
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ENST00000675648.1:n.1379A>T
|
|
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ENST00000675916.1:c.248A>T
|
|
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ENST00000676173.1:n.2749A>T
|
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ENST00000676182.1:c.435A>T
|
|
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ENST00000676228.1:c.*1327A>T
|
ENSP00000502375.1:n.*1327A>T
|
|
ENST00000255078.7:c.2004A>T
|
ENSP00000255078.3:p.Gly668=
|
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ENST00000539064.5:n.1763A>T
|
|
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ENST00000543739.5:n.997A>T
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NM_002180.2:c.2004A>T , LRG_250t1:c.2004A>T
|
NP_002171.2:p.Gly668=
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|
XM_005273974.2:c.993A>T
|
XP_005274031.1:p.Gly331=
|
|
XM_005273975.2:c.876A>T
|
XP_005274032.1:p.Gly292=
|
|
XM_011544994.1:c.771A>T
|
XP_011543296.1:p.Gly257=
|
|
XR_949903.1:n.2106A>T
|
|
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XM_005273975.3:c.876A>T
|
XP_005274032.1:p.Gly292=
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|
XM_017017669.2:c.993A>T
|
XP_016873158.1:p.Gly331=
|
|
XM_017017670.2:c.993A>T
|
XP_016873159.1:p.Gly331=
|
|
XR_949903.3:n.2102A>T
|
|
|
NM_002180.3:c.2004A>T
MANE Select
|
NP_002171.2:p.Gly668=
|
|