ENST00000370096.9:c.2622C>G
MANE Select
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ENSP00000359114.3:p.Gly874=
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ENST00000353414.8:c.2505C>G
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ENSP00000302551.6:p.Gly835=
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ENST00000358392.6:c.2658C>G
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ENSP00000351163.2:p.Gly886=
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ENST00000370096.7:c.2622C>G
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ENSP00000359114.3:p.Gly874=
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ENST00000512756.5:c.2274C>G
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ENSP00000426533.1:p.Gly758=
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ENST00000635193.1:c.1956C>G
|
|
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NM_001190709.1:c.2505C>G
|
NP_001177638.1:p.Gly835=
|
|
NM_001854.3:c.2622C>G
|
NP_001845.3:p.Gly874=
|
|
NM_080629.2:c.2658C>G
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NP_542196.2:p.Gly886=
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NM_080630.3:c.2274C>G
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NP_542197.3:p.Gly758=
|
|
XM_011540719.1:c.2622C>G
|
XP_011539021.1:p.Gly874=
|
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XM_011540720.1:c.855C>G
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XP_011539022.1:p.Gly285=
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XM_011540721.1:c.210C>G
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XP_011539023.1:p.Gly70=
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XR_946545.1:n.3036C>G
|
|
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NR_134980.1:n.2956C>G
|
|
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XM_017000334.1:c.2775C>G
|
XP_016855823.1:p.Gly925=
|
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XM_017000335.1:c.2769C>G
|
XP_016855824.1:p.Gly923=
|
|
XM_017000336.1:c.2775C>G
|
XP_016855825.1:p.Gly925=
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XM_017000337.1:c.1173C>G
|
XP_016855826.1:p.Gly391=
|
|
NM_001854.4:c.2622C>G
MANE Select
|
NP_001845.3:p.Gly874=
|
|
NM_080630.4:c.2274C>G
|
NP_542197.3:p.Gly758=
|
|
NR_134980.2:n.2982C>G
|
|
|
NM_001190709.2:c.2505C>G
|
NP_001177638.1:p.Gly835=
|
|
NM_080629.3:c.2658C>G
|
NP_542196.2:p.Gly886=
|
|