ENST00000368485.8:c.1188T>A
MANE Select
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ENSP00000357470.3:p.Ala396=
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ENST00000344086.8:c.1094T>A
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ENSP00000340589.4:p.Leu365His
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ENST00000368485.7:c.1188T>A
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ENSP00000357470.3:p.Ala396=
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ENST00000502679.1:n.501T>A
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ENST00000507256.1:n.386T>A
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NM_000565.3:c.1188T>A
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NP_000556.1:p.Ala396=
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NM_181359.2:c.1094T>A
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NP_852004.1:p.Leu365His
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XM_005245139.1:c.952T>A
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XP_005245196.1:p.Ser318Thr
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XM_005245140.1:c.*29T>A
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XP_005245197.1:n.*29T>A
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XM_006711298.1:c.1236T>A
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XP_006711361.1:p.Ala412=
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XM_006711299.2:c.1142T>A
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XP_006711362.1:p.Leu381His
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XM_005245139.2:c.952T>A
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XP_005245196.1:p.Ser318Thr
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XM_005245140.3:c.*29T>A
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XP_005245197.1:n.*29T>A
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XM_006711298.2:c.1236T>A
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XP_006711361.1:p.Ala412=
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XM_006711299.4:c.1142T>A
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XP_006711362.1:p.Leu381His
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XM_017001199.2:c.1335T>A
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XP_016856688.1:p.Ala445=
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XM_017001200.2:c.1287T>A
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XP_016856689.1:p.Ala429=
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XM_017001201.2:c.*29T>A
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XP_016856690.1:n.*29T>A
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NM_000565.4:c.1188T>A
MANE Select
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NP_000556.1:p.Ala396=
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NM_181359.3:c.1094T>A
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NP_852004.1:p.Leu365His
|
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NM_001382769.1:c.1287T>A
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NP_001369698.1:p.Ala429=
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NM_001382770.1:c.1281T>A
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NP_001369699.1:p.Ala427=
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NM_001382771.1:c.1236T>A
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NP_001369700.1:p.Ala412=
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NM_001382772.1:c.1182T>A
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NP_001369701.1:p.Ala394=
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NM_001382773.1:c.1142T>A
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NP_001369702.1:p.Leu381His
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NM_001382774.1:c.828T>A
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NP_001369703.1:p.Ala276=
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