ENST00000368485.8:c.1201A>G
MANE Select
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ENSP00000357470.3:p.Lys401Glu
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ENST00000344086.8:c.*9A>G
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ENSP00000340589.4:n.*9A>G
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ENST00000368485.7:c.1201A>G
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ENSP00000357470.3:p.Lys401Glu
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ENST00000502679.1:n.514A>G
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ENST00000507256.1:n.399A>G
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NM_000565.3:c.1201A>G
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NP_000556.1:p.Lys401Glu
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NM_181359.2:c.*9A>G
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NP_852004.1:n.*9A>G
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XM_005245139.1:c.965A>G
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XP_005245196.1:p.Gln322Arg
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XM_005245140.1:c.*42A>G
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XP_005245197.1:n.*42A>G
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XM_006711298.1:c.1249A>G
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XP_006711361.1:p.Lys417Glu
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XM_006711299.2:c.*9A>G
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XP_006711362.1:n.*9A>G
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XM_005245139.2:c.965A>G
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XP_005245196.1:p.Gln322Arg
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XM_005245140.3:c.*42A>G
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XP_005245197.1:n.*42A>G
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XM_006711298.2:c.1249A>G
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XP_006711361.1:p.Lys417Glu
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XM_006711299.4:c.*9A>G
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XP_006711362.1:n.*9A>G
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XM_017001199.2:c.1348A>G
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XP_016856688.1:p.Lys450Glu
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XM_017001200.2:c.1300A>G
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XP_016856689.1:p.Lys434Glu
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XM_017001201.2:c.*42A>G
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XP_016856690.1:n.*42A>G
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NM_000565.4:c.1201A>G
MANE Select
|
NP_000556.1:p.Lys401Glu
|
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NM_181359.3:c.*9A>G
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NP_852004.1:n.*9A>G
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NM_001382769.1:c.1300A>G
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NP_001369698.1:p.Lys434Glu
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NM_001382770.1:c.1294A>G
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NP_001369699.1:p.Lys432Glu
|
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NM_001382771.1:c.1249A>G
|
NP_001369700.1:p.Lys417Glu
|
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NM_001382772.1:c.1195A>G
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NP_001369701.1:p.Lys399Glu
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NM_001382773.1:c.*9A>G
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NP_001369702.1:n.*9A>G
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NM_001382774.1:c.841A>G
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NP_001369703.1:p.Lys281Glu
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