ENST00000368485.8:c.1232G>T
MANE Select
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ENSP00000357470.3:p.Gly411Val
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ENST00000344086.8:c.*40G>T
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ENSP00000340589.4:n.*40G>T
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ENST00000368485.7:c.1232G>T
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ENSP00000357470.3:p.Gly411Val
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ENST00000502679.1:n.545G>T
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ENST00000507256.1:n.430G>T
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NM_000565.3:c.1232G>T
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NP_000556.1:p.Gly411Val
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NM_181359.2:c.*40G>T
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NP_852004.1:n.*40G>T
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XM_005245139.1:c.996G>T
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XP_005245196.1:p.Gly332=
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XM_005245140.1:c.*73G>T
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XP_005245197.1:n.*73G>T
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XM_006711298.1:c.1280G>T
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XP_006711361.1:p.Gly427Val
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XM_006711299.2:c.*40G>T
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XP_006711362.1:n.*40G>T
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XM_005245139.2:c.996G>T
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XP_005245196.1:p.Gly332=
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XM_005245140.3:c.*73G>T
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XP_005245197.1:n.*73G>T
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XM_006711298.2:c.1280G>T
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XP_006711361.1:p.Gly427Val
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XM_006711299.4:c.*40G>T
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XP_006711362.1:n.*40G>T
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XM_017001199.2:c.1379G>T
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XP_016856688.1:p.Gly460Val
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XM_017001200.2:c.1331G>T
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XP_016856689.1:p.Gly444Val
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XM_017001201.2:c.*73G>T
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XP_016856690.1:n.*73G>T
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NM_000565.4:c.1232G>T
MANE Select
|
NP_000556.1:p.Gly411Val
|
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NM_181359.3:c.*40G>T
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NP_852004.1:n.*40G>T
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NM_001382769.1:c.1331G>T
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NP_001369698.1:p.Gly444Val
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NM_001382770.1:c.1325G>T
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NP_001369699.1:p.Gly442Val
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NM_001382771.1:c.1280G>T
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NP_001369700.1:p.Gly427Val
|
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NM_001382772.1:c.1226G>T
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NP_001369701.1:p.Gly409Val
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NM_001382773.1:c.*40G>T
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NP_001369702.1:n.*40G>T
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NM_001382774.1:c.872G>T
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NP_001369703.1:p.Gly291Val
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