ENST00000368485.8:c.1166A>T
MANE Select
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ENSP00000357470.3:p.Lys389Met
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ENST00000344086.8:c.1072A>T
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ENSP00000340589.4:p.Arg358Ter
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ENST00000368485.7:c.1166A>T
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ENSP00000357470.3:p.Lys389Met
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ENST00000502679.1:n.479A>T
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|
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ENST00000507256.1:n.364A>T
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|
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NM_000565.3:c.1166A>T
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NP_000556.1:p.Lys389Met
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NM_181359.2:c.1072A>T
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NP_852004.1:p.Arg358Ter
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XM_005245139.1:c.930A>T
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XP_005245196.1:p.Gln310His
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XM_005245140.1:c.*7A>T
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XP_005245197.1:n.*7A>T
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XM_006711298.1:c.1214A>T
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XP_006711361.1:p.Lys405Met
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XM_006711299.2:c.1120A>T
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XP_006711362.1:p.Arg374Ter
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XM_005245139.2:c.930A>T
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XP_005245196.1:p.Gln310His
|
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XM_005245140.3:c.*7A>T
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XP_005245197.1:n.*7A>T
|
|
XM_006711298.2:c.1214A>T
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XP_006711361.1:p.Lys405Met
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XM_006711299.4:c.1120A>T
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XP_006711362.1:p.Arg374Ter
|
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XM_017001199.2:c.1313A>T
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XP_016856688.1:p.Lys438Met
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XM_017001200.2:c.1265A>T
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XP_016856689.1:p.Lys422Met
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XM_017001201.2:c.*7A>T
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XP_016856690.1:n.*7A>T
|
|
NM_000565.4:c.1166A>T
MANE Select
|
NP_000556.1:p.Lys389Met
|
|
NM_181359.3:c.1072A>T
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NP_852004.1:p.Arg358Ter
|
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NM_001382769.1:c.1265A>T
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NP_001369698.1:p.Lys422Met
|
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NM_001382770.1:c.1259A>T
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NP_001369699.1:p.Lys420Met
|
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NM_001382771.1:c.1214A>T
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NP_001369700.1:p.Lys405Met
|
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NM_001382772.1:c.1160A>T
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NP_001369701.1:p.Lys387Met
|
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NM_001382773.1:c.1120A>T
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NP_001369702.1:p.Arg374Ter
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NM_001382774.1:c.806A>T
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NP_001369703.1:p.Lys269Met
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