ENST00000370096.9:c.2631C>A
MANE Select
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ENSP00000359114.3:p.Gly877=
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ENST00000353414.8:c.2514C>A
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ENSP00000302551.6:p.Gly838=
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ENST00000358392.6:c.2667C>A
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ENSP00000351163.2:p.Gly889=
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ENST00000370096.7:c.2631C>A
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ENSP00000359114.3:p.Gly877=
|
|
ENST00000512756.5:c.2283C>A
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ENSP00000426533.1:p.Gly761=
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ENST00000635193.1:c.1965C>A
|
|
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NM_001190709.1:c.2514C>A
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NP_001177638.1:p.Gly838=
|
|
NM_001854.3:c.2631C>A
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NP_001845.3:p.Gly877=
|
|
NM_080629.2:c.2667C>A
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NP_542196.2:p.Gly889=
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|
NM_080630.3:c.2283C>A
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NP_542197.3:p.Gly761=
|
|
XM_011540719.1:c.2631C>A
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XP_011539021.1:p.Gly877=
|
|
XM_011540720.1:c.864C>A
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XP_011539022.1:p.Gly288=
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XM_011540721.1:c.219C>A
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XP_011539023.1:p.Gly73=
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XR_946545.1:n.3045C>A
|
|
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NR_134980.1:n.2965C>A
|
|
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XM_017000334.1:c.2784C>A
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XP_016855823.1:p.Gly928=
|
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XM_017000335.1:c.2778C>A
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XP_016855824.1:p.Gly926=
|
|
XM_017000336.1:c.2784C>A
|
XP_016855825.1:p.Gly928=
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|
XM_017000337.1:c.1182C>A
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XP_016855826.1:p.Gly394=
|
|
NM_001854.4:c.2631C>A
MANE Select
|
NP_001845.3:p.Gly877=
|
|
NM_080630.4:c.2283C>A
|
NP_542197.3:p.Gly761=
|
|
NR_134980.2:n.2991C>A
|
|
|
NM_001190709.2:c.2514C>A
|
NP_001177638.1:p.Gly838=
|
|
NM_080629.3:c.2667C>A
|
NP_542196.2:p.Gly889=
|
|