ENST00000370096.9:c.2613A>T
MANE Select
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ENSP00000359114.3:p.Gly871=
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ENST00000353414.8:c.2496A>T
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ENSP00000302551.6:p.Gly832=
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ENST00000358392.6:c.2649A>T
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ENSP00000351163.2:p.Gly883=
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ENST00000370096.7:c.2613A>T
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ENSP00000359114.3:p.Gly871=
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ENST00000512756.5:c.2265A>T
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ENSP00000426533.1:p.Gly755=
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ENST00000635193.1:c.1947A>T
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NM_001190709.1:c.2496A>T
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NP_001177638.1:p.Gly832=
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NM_001854.3:c.2613A>T
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NP_001845.3:p.Gly871=
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NM_080629.2:c.2649A>T
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NP_542196.2:p.Gly883=
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NM_080630.3:c.2265A>T
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NP_542197.3:p.Gly755=
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XM_011540719.1:c.2613A>T
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XP_011539021.1:p.Gly871=
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XM_011540720.1:c.846A>T
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XP_011539022.1:p.Gly282=
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XM_011540721.1:c.201A>T
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XP_011539023.1:p.Gly67=
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XR_946545.1:n.3027A>T
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NR_134980.1:n.2947A>T
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|
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XM_017000334.1:c.2766A>T
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XP_016855823.1:p.Gly922=
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XM_017000335.1:c.2760A>T
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XP_016855824.1:p.Gly920=
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XM_017000336.1:c.2766A>T
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XP_016855825.1:p.Gly922=
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XM_017000337.1:c.1164A>T
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XP_016855826.1:p.Gly388=
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NM_001854.4:c.2613A>T
MANE Select
|
NP_001845.3:p.Gly871=
|
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NM_080630.4:c.2265A>T
|
NP_542197.3:p.Gly755=
|
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NR_134980.2:n.2973A>T
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|
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NM_001190709.2:c.2496A>T
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NP_001177638.1:p.Gly832=
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NM_080629.3:c.2649A>T
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NP_542196.2:p.Gly883=
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