ENST00000261304.7:c.651T=
MANE Select
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ENSP00000261304.2:p.Gly217=
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ENST00000261304.6:c.651T=
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ENSP00000261304.2:p.Gly217=
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|
ENST00000393568.8:c.582T=
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ENSP00000377198.4:p.Gly194=
|
|
ENST00000393569.6:c.573T=
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ENSP00000377199.2:p.Gly191=
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|
ENST00000474294.6:n.641T=
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|
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ENST00000477716.3:n.406T=
|
|
|
ENST00000544807.6:c.483T=
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ENSP00000437513.2:p.Gly161=
|
|
ENST00000554916.5:n.530T=
|
|
|
ENST00000555000.5:c.18T=
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ENSP00000450472.1:p.Gly6=
|
|
ENST00000557316.5:c.*49T=
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ENSP00000452314.1:n.*49T=
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|
ENST00000622264.4:c.641T=
|
|
|
NM_000153.3:c.651T=
|
NP_000144.2:p.Gly217=
|
|
NM_001201401.1:c.582T=
|
NP_001188330.1:p.Gly194=
|
|
NM_001201402.1:c.573T=
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NP_001188331.1:p.Gly191=
|
|
XM_011536618.1:c.483T=
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XP_011534920.1:p.Gly161=
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|
XM_011536618.2:c.483T=
|
XP_011534920.1:p.Gly161=
|
|
NM_000153.4:c.651T=
MANE Select
|
NP_000144.2:p.Gly217=
|
|
NM_001201401.2:c.582T=
|
NP_001188330.1:p.Gly194=
|
|
NM_001201402.2:c.573T=
|
NP_001188331.1:p.Gly191=
|
|