ENST00000265104.5:c.8002G>T
MANE Select
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ENSP00000265104.4:p.Gly2668Ter
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ENST00000681290.1:c.7957G>T
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ENSP00000505288.1:p.Gly2653Ter
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ENST00000265104.4:c.8002G>T
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ENSP00000265104.4:p.Gly2668Ter
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NM_001369.2:c.8002G>T
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NP_001360.1:p.Gly2668Ter
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XM_005248262.2:c.7957G>T
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XP_005248319.1:p.Gly2653Ter
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XM_011513990.1:c.8002G>T
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XP_011512292.1:p.Gly2668Ter
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XR_925598.1:n.8209G>T
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XM_005248262.3:c.8110G>T
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XP_005248319.2:p.Gly2704Ter
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XM_017009177.1:c.8110G>T
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XP_016864666.1:p.Gly2704Ter
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XM_017009178.1:c.7015G>T
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XP_016864667.1:p.Gly2339Ter
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XM_017009179.2:c.7015G>T
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XP_016864668.1:p.Gly2339Ter
|
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XM_017009180.1:c.8110G>T
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XP_016864669.1:p.Gly2704Ter
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XM_017009181.1:c.8110G>T
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XP_016864670.1:p.Gly2704Ter
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XM_017009182.1:c.8110G>T
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XP_016864671.1:p.Gly2704Ter
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XM_017009183.1:c.8110G>T
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XP_016864672.1:p.Gly2704Ter
|
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XM_017009184.1:c.8110G>T
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XP_016864673.1:p.Gly2704Ter
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XM_017009185.1:c.3199G>T
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XP_016864674.1:p.Gly1067Ter
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XM_017009186.1:c.2752G>T
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XP_016864675.1:p.Gly918Ter
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XM_017009188.1:c.2089G>T
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XP_016864677.1:p.Gly697Ter
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XM_024454388.1:c.7015G>T
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XP_024310156.1:p.Gly2339Ter
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XM_024454389.1:c.6604G>T
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XP_024310157.1:p.Gly2202Ter
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XR_001742034.1:n.8127G>T
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XR_001742035.1:n.8127G>T
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NM_001369.3:c.8002G>T
MANE Select
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NP_001360.1:p.Gly2668Ter
|
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