ENST00000290866.10:c.3507C>T
MANE Select
|
ENSP00000290866.4:p.Thr1169=
|
|
ENST00000290863.10:c.1785C>T
|
ENSP00000290863.6:p.Thr595=
|
|
ENST00000290866.9:c.3507C>T
|
ENSP00000290866.4:p.Thr1169=
|
|
ENST00000413513.7:c.1662C>T
|
ENSP00000392247.3:p.Thr554=
|
|
ENST00000428043.5:c.3507C>T
|
ENSP00000397593.2:p.Thr1169=
|
|
ENST00000577418.5:n.517C>T
|
|
|
ENST00000577647.2:c.1785C>T
|
ENSP00000464149.1:p.Thr595=
|
|
ENST00000578839.5:c.*1262C>T
|
ENSP00000462110.2:n.*1262C>T
|
|
ENST00000579314.5:c.*1236C>T
|
ENSP00000462599.1:n.*1236C>T
|
|
ENST00000579409.1:c.194C>T
|
|
|
ENST00000582244.1:n.381C>T
|
|
|
NM_000789.3:c.3507C>T
|
NP_000780.1:p.Thr1169=
|
|
NM_001178057.1:c.1662C>T
|
NP_001171528.1:p.Thr554=
|
|
NM_152830.2:c.1785C>T
|
NP_690043.1:p.Thr595=
|
|
XM_005257110.1:c.2958C>T
|
XP_005257167.1:p.Thr986=
|
|
XM_006721737.2:c.1845C>T
|
XP_006721800.2:p.Thr615=
|
|
XM_006721737.3:c.1845C>T
|
XP_006721800.2:p.Thr615=
|
|
NM_000789.4:c.3507C>T
MANE Select
|
NP_000780.1:p.Thr1169=
|
|
NM_001178057.2:c.1662C>T
|
NP_001171528.1:p.Thr554=
|
|
NM_152830.3:c.1785C>T
|
NP_690043.1:p.Thr595=
|
|
NM_001382700.1:c.2940C>T
|
NP_001369629.1:p.Thr980=
|
|
NM_001382701.1:c.2655C>T
|
NP_001369630.1:p.Thr885=
|
|
NM_001382702.1:c.1122C>T
|
NP_001369631.1:p.Thr374=
|
|
NR_168483.1:n.1885C>T
|
|
|