ENST00000682089.1:n.202T>C
|
|
|
ENST00000682266.1:c.432T>C
|
ENSP00000507766.1:p.Asn144=
|
|
ENST00000682341.1:c.840T>C
|
ENSP00000508251.1:p.Asn280=
|
|
ENST00000682530.1:c.*814T>C
|
ENSP00000506805.1:n.*814T>C
|
|
ENST00000683197.1:c.840T>C
|
ENSP00000507641.1:p.Asn280=
|
|
ENST00000683411.1:c.432T>C
|
ENSP00000508397.1:p.Asn144=
|
|
ENST00000683437.1:c.432T>C
|
ENSP00000508408.1:p.Asn144=
|
|
ENST00000683613.1:n.1876T>C
|
|
|
ENST00000683834.1:n.1082T>C
|
|
|
ENST00000684663.1:c.837T>C
|
ENSP00000508009.1:p.Asn279=
|
|
ENST00000324559.9:c.882T>C
MANE Select
|
ENSP00000315371.9:p.Asn294=
|
|
ENST00000648804.1:n.1217T>C
|
|
|
ENST00000324559.8:c.882T>C
|
ENSP00000315371.8:p.Asn294=
|
|
NM_001142649.1:c.879T>C
|
NP_001136121.1:p.Asn293=
|
|
NM_213599.2:c.882T>C , LRG_868t1:c.882T>C
|
NP_998764.1:p.Asn294=
|
|
XM_005252820.2:c.840T>C
|
XP_005252877.2:p.Asn280=
|
|
XM_005252821.2:c.837T>C
|
XP_005252878.2:p.Asn279=
|
|
XM_005252822.3:c.804T>C
|
XP_005252879.1:p.Asn268=
|
|
XM_005252823.3:c.801T>C
|
XP_005252880.1:p.Asn267=
|
|
XM_011519949.1:c.789T>C
|
XP_011518251.1:p.Asn263=
|
|
XM_005252820.3:c.840T>C
|
XP_005252877.2:p.Asn280=
|
|
XM_005252821.3:c.837T>C
|
XP_005252878.2:p.Asn279=
|
|
XM_005252822.4:c.804T>C
|
XP_005252879.1:p.Asn268=
|
|
XM_011519949.2:c.789T>C
|
XP_011518251.1:p.Asn263=
|
|
NM_001142649.2:c.879T>C
|
NP_001136121.1:p.Asn293=
|
|
NM_213599.3:c.882T>C
MANE Select
|
NP_998764.1:p.Asn294=
|
|