ENST00000368485.8:c.1328C>G
MANE Select
|
ENSP00000357470.3:p.Ser443Trp
|
|
ENST00000344086.8:c.*136C>G
|
ENSP00000340589.4:n.*136C>G
|
|
ENST00000368485.7:c.1328C>G
|
ENSP00000357470.3:p.Ser443Trp
|
|
ENST00000507256.1:n.526C>G
|
|
|
NM_000565.3:c.1328C>G
|
NP_000556.1:p.Ser443Trp
|
|
NM_181359.2:c.*136C>G
|
NP_852004.1:n.*136C>G
|
|
XM_005245139.1:c.*9C>G
|
XP_005245196.1:n.*9C>G
|
|
XM_005245140.1:c.*169C>G
|
XP_005245197.1:n.*169C>G
|
|
XM_006711298.1:c.1376C>G
|
XP_006711361.1:p.Ser459Trp
|
|
XM_005245139.2:c.*9C>G
|
XP_005245196.1:n.*9C>G
|
|
XM_005245140.3:c.*169C>G
|
XP_005245197.1:n.*169C>G
|
|
XM_006711298.2:c.1376C>G
|
XP_006711361.1:p.Ser459Trp
|
|
XM_017001199.2:c.1475C>G
|
XP_016856688.1:p.Ser492Trp
|
|
XM_017001200.2:c.1427C>G
|
XP_016856689.1:p.Ser476Trp
|
|
XM_017001201.2:c.*169C>G
|
XP_016856690.1:n.*169C>G
|
|
NM_000565.4:c.1328C>G
MANE Select
|
NP_000556.1:p.Ser443Trp
|
|
NM_181359.3:c.*136C>G
|
NP_852004.1:n.*136C>G
|
|
NM_001382769.1:c.1427C>G
|
NP_001369698.1:p.Ser476Trp
|
|
NM_001382770.1:c.1421C>G
|
NP_001369699.1:p.Ser474Trp
|
|
NM_001382771.1:c.1376C>G
|
NP_001369700.1:p.Ser459Trp
|
|
NM_001382772.1:c.1322C>G
|
NP_001369701.1:p.Ser441Trp
|
|
NM_001382773.1:c.*136C>G
|
NP_001369702.1:n.*136C>G
|
|
NM_001382774.1:c.968C>G
|
NP_001369703.1:p.Ser323Trp
|
|