ENST00000262367.10:c.5312G>C
MANE Select
|
ENSP00000262367.5:p.Ser1771Thr
|
|
ENST00000262367.9:c.5312G>C
|
ENSP00000262367.5:p.Ser1771Thr
|
|
ENST00000382070.7:c.5198G>C
|
ENSP00000371502.3:p.Ser1733Thr
|
|
NM_001079846.1:c.5198G>C
|
NP_001073315.1:p.Ser1733Thr
|
|
NM_004380.2:c.5312G>C
|
NP_004371.2:p.Ser1771Thr
|
|
XM_005255124.3:c.5267G>C
|
XP_005255181.1:p.Ser1756Thr
|
|
XM_005255125.3:c.4895G>C
|
XP_005255182.1:p.Ser1632Thr
|
|
XM_006720848.2:c.5051G>C
|
XP_006720911.1:p.Ser1684Thr
|
|
XM_011522380.1:c.5258G>C
|
XP_011520682.1:p.Ser1753Thr
|
|
XM_011522381.1:c.4559G>C
|
XP_011520683.1:p.Ser1520Thr
|
|
XM_005255124.4:c.5267G>C
|
XP_005255181.1:p.Ser1756Thr
|
|
XM_005255125.4:c.4895G>C
|
XP_005255182.1:p.Ser1632Thr
|
|
XM_006720848.3:c.5051G>C
|
XP_006720911.1:p.Ser1684Thr
|
|
XM_011522381.2:c.4559G>C
|
XP_011520683.1:p.Ser1520Thr
|
|
XM_017022944.1:c.5306G>C
|
XP_016878433.1:p.Ser1769Thr
|
|
NM_004380.3:c.5312G>C
MANE Select
|
NP_004371.2:p.Ser1771Thr
|
|