ENST00000368485.8:c.1381A>C
MANE Select
|
ENSP00000357470.3:p.Asn461His
|
|
ENST00000344086.8:c.*189A>C
|
ENSP00000340589.4:n.*189A>C
|
|
ENST00000368485.7:c.1381A>C
|
ENSP00000357470.3:p.Asn461His
|
|
NM_000565.3:c.1381A>C
|
NP_000556.1:p.Asn461His
|
|
NM_181359.2:c.*189A>C
|
NP_852004.1:n.*189A>C
|
|
XM_005245139.1:c.*62A>C
|
XP_005245196.1:n.*62A>C
|
|
XM_005245140.1:c.*222A>C
|
XP_005245197.1:n.*222A>C
|
|
XM_006711298.1:c.1429A>C
|
XP_006711361.1:p.Asn477His
|
|
XM_005245139.2:c.*62A>C
|
XP_005245196.1:n.*62A>C
|
|
XM_005245140.3:c.*222A>C
|
XP_005245197.1:n.*222A>C
|
|
XM_006711298.2:c.1429A>C
|
XP_006711361.1:p.Asn477His
|
|
XM_017001199.2:c.1528A>C
|
XP_016856688.1:p.Asn510His
|
|
XM_017001200.2:c.1480A>C
|
XP_016856689.1:p.Asn494His
|
|
XM_017001201.2:c.*222A>C
|
XP_016856690.1:n.*222A>C
|
|
NM_000565.4:c.1381A>C
MANE Select
|
NP_000556.1:p.Asn461His
|
|
NM_181359.3:c.*189A>C
|
NP_852004.1:n.*189A>C
|
|
NM_001382769.1:c.1480A>C
|
NP_001369698.1:p.Asn494His
|
|
NM_001382770.1:c.1474A>C
|
NP_001369699.1:p.Asn492His
|
|
NM_001382771.1:c.1429A>C
|
NP_001369700.1:p.Asn477His
|
|
NM_001382772.1:c.1375A>C
|
NP_001369701.1:p.Asn459His
|
|
NM_001382773.1:c.*189A>C
|
NP_001369702.1:n.*189A>C
|
|
NM_001382774.1:c.1021A>C
|
NP_001369703.1:p.Asn341His
|
|