ENST00000368485.8:c.1261A>G
MANE Select
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ENSP00000357470.3:p.Thr421Ala
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ENST00000344086.8:c.*69A>G
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ENSP00000340589.4:n.*69A>G
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ENST00000368485.7:c.1261A>G
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ENSP00000357470.3:p.Thr421Ala
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ENST00000502679.1:n.574A>G
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ENST00000507256.1:n.459A>G
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NM_000565.3:c.1261A>G
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NP_000556.1:p.Thr421Ala
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NM_181359.2:c.*69A>G
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NP_852004.1:n.*69A>G
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XM_005245139.1:c.1025A>G
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XP_005245196.1:p.His342Arg
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XM_005245140.1:c.*102A>G
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XP_005245197.1:n.*102A>G
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XM_006711298.1:c.1309A>G
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XP_006711361.1:p.Thr437Ala
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XM_006711299.2:c.*69A>G
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XP_006711362.1:n.*69A>G
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XM_005245139.2:c.1025A>G
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XP_005245196.1:p.His342Arg
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XM_005245140.3:c.*102A>G
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XP_005245197.1:n.*102A>G
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XM_006711298.2:c.1309A>G
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XP_006711361.1:p.Thr437Ala
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XM_006711299.4:c.*69A>G
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XP_006711362.1:n.*69A>G
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XM_017001199.2:c.1408A>G
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XP_016856688.1:p.Thr470Ala
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XM_017001200.2:c.1360A>G
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XP_016856689.1:p.Thr454Ala
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XM_017001201.2:c.*102A>G
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XP_016856690.1:n.*102A>G
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NM_000565.4:c.1261A>G
MANE Select
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NP_000556.1:p.Thr421Ala
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NM_181359.3:c.*69A>G
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NP_852004.1:n.*69A>G
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NM_001382769.1:c.1360A>G
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NP_001369698.1:p.Thr454Ala
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NM_001382770.1:c.1354A>G
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NP_001369699.1:p.Thr452Ala
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NM_001382771.1:c.1309A>G
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NP_001369700.1:p.Thr437Ala
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NM_001382772.1:c.1255A>G
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NP_001369701.1:p.Thr419Ala
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NM_001382773.1:c.*69A>G
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NP_001369702.1:n.*69A>G
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NM_001382774.1:c.901A>G
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NP_001369703.1:p.Thr301Ala
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