ENST00000368485.8:c.1175G>C
MANE Select
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ENSP00000357470.3:p.Trp392Ser
|
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ENST00000344086.8:c.1081G>C
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ENSP00000340589.4:p.Gly361Arg
|
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ENST00000368485.7:c.1175G>C
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ENSP00000357470.3:p.Trp392Ser
|
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ENST00000502679.1:n.488G>C
|
|
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ENST00000507256.1:n.373G>C
|
|
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NM_000565.3:c.1175G>C
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NP_000556.1:p.Trp392Ser
|
|
NM_181359.2:c.1081G>C
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NP_852004.1:p.Gly361Arg
|
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XM_005245139.1:c.939G>C
|
XP_005245196.1:p.Val313=
|
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XM_005245140.1:c.*16G>C
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XP_005245197.1:n.*16G>C
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XM_006711298.1:c.1223G>C
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XP_006711361.1:p.Trp408Ser
|
|
XM_006711299.2:c.1129G>C
|
XP_006711362.1:p.Gly377Arg
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|
XM_005245139.2:c.939G>C
|
XP_005245196.1:p.Val313=
|
|
XM_005245140.3:c.*16G>C
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XP_005245197.1:n.*16G>C
|
|
XM_006711298.2:c.1223G>C
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XP_006711361.1:p.Trp408Ser
|
|
XM_006711299.4:c.1129G>C
|
XP_006711362.1:p.Gly377Arg
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|
XM_017001199.2:c.1322G>C
|
XP_016856688.1:p.Trp441Ser
|
|
XM_017001200.2:c.1274G>C
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XP_016856689.1:p.Trp425Ser
|
|
XM_017001201.2:c.*16G>C
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XP_016856690.1:n.*16G>C
|
|
NM_000565.4:c.1175G>C
MANE Select
|
NP_000556.1:p.Trp392Ser
|
|
NM_181359.3:c.1081G>C
|
NP_852004.1:p.Gly361Arg
|
|
NM_001382769.1:c.1274G>C
|
NP_001369698.1:p.Trp425Ser
|
|
NM_001382770.1:c.1268G>C
|
NP_001369699.1:p.Trp423Ser
|
|
NM_001382771.1:c.1223G>C
|
NP_001369700.1:p.Trp408Ser
|
|
NM_001382772.1:c.1169G>C
|
NP_001369701.1:p.Trp390Ser
|
|
NM_001382773.1:c.1129G>C
|
NP_001369702.1:p.Gly377Arg
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|
NM_001382774.1:c.815G>C
|
NP_001369703.1:p.Trp272Ser
|
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