ENST00000233202.11:c.1642A>G
MANE Select
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ENSP00000233202.6:p.Thr548Ala
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ENST00000233202.10:c.1642A>G
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ENSP00000233202.6:p.Thr548Ala
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ENST00000354352.9:c.*1224A>G
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ENSP00000346320.5:n.*1224A>G
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ENST00000465984.5:n.2118A>G
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ENST00000468221.5:n.4769A>G
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NM_000578.3:c.1642A>G
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NP_000569.3:p.Thr548Ala
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XM_005246793.2:c.1441A>G
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XP_005246850.1:p.Thr481Ala
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XM_005246794.2:c.1288A>G
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XP_005246851.1:p.Thr430Ala
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XM_006712709.2:c.1288A>G
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XP_006712772.1:p.Thr430Ala
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XM_006712710.2:c.1288A>G
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XP_006712773.1:p.Thr430Ala
|
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XM_006712711.2:c.1195A>G
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XP_006712774.1:p.Thr399Ala
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XM_011511684.1:c.1315A>G
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XP_011509986.1:p.Thr439Ala
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XM_011511685.1:c.1315A>G
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XP_011509987.1:p.Thr439Ala
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XM_005246793.4:c.1441A>G
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XP_005246850.1:p.Thr481Ala
|
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XM_005246794.4:c.1288A>G
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XP_005246851.1:p.Thr430Ala
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XM_006712709.4:c.1288A>G
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XP_006712772.1:p.Thr430Ala
|
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XM_006712710.4:c.1288A>G
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XP_006712773.1:p.Thr430Ala
|
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XM_006712711.4:c.1195A>G
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XP_006712774.1:p.Thr399Ala
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XM_011511684.3:c.1315A>G
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XP_011509986.1:p.Thr439Ala
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XM_011511685.3:c.1315A>G
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XP_011509987.1:p.Thr439Ala
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XM_017004765.2:c.1519A>G
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XP_016860254.1:p.Thr507Ala
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XM_017004766.2:c.1441A>G
|
XP_016860255.1:p.Thr481Ala
|
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XM_017004767.2:c.1273A>G
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XP_016860256.1:p.Thr425Ala
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XR_427107.3:n.2657A>G
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XR_427108.4:n.2968A>G
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NM_000578.4:c.1642A>G
MANE Select
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NP_000569.3:p.Thr548Ala
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