ENST00000370192.8:c.226G>A
MANE Select
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ENSP00000359211.3:p.Ala76Thr
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ENST00000306031.5:c.226G>A
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ENSP00000307107.5:p.Ala76Thr
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ENST00000370192.7:c.226G>A
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ENSP00000359211.3:p.Ala76Thr
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NM_000110.3:c.226G>A , LRG_722t1:c.226G>A
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NP_000101.2:p.Ala76Thr
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NM_001160301.1:c.226G>A , LRG_722t2:c.226G>A
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NP_001153773.1:p.Ala76Thr
|
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XM_005270562.3:c.226G>A
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XP_005270619.2:p.Ala76Thr
|
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XM_006710397.2:c.226G>A
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XP_006710460.1:p.Ala76Thr
|
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XM_006710397.3:c.226G>A
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XP_006710460.1:p.Ala76Thr
|
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XM_017000507.1:c.115G>A
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XP_016855996.1:p.Ala39Thr
|
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XM_017000508.2:c.-485G>A
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XP_016855997.1:n.-485G>A
|
|
XM_017000509.2:c.-383G>A
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XP_016855998.1:n.-383G>A
|
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XM_017000510.1:c.-383G>A
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XP_016855999.1:n.-383G>A
|
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XR_001737014.1:n.363G>A
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|
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NM_000110.4:c.226G>A
MANE Select
|
NP_000101.2:p.Ala76Thr
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