ENST00000373207.2:c.2984G>C
MANE Select
|
ENSP00000362303.1:p.Cys995Ser
|
|
ENST00000373207.1:c.2984G>C
|
ENSP00000362303.1:p.Cys995Ser
|
|
ENST00000373208.5:c.2993G>C
|
ENSP00000362304.1:p.Cys998Ser
|
|
NM_080722.3:c.2984G>C
|
NP_542453.2:p.Cys995Ser
|
|
NM_139155.2:c.2993G>C
|
NP_631894.2:p.Cys998Ser
|
|
XM_011539300.1:c.2483G>C
|
XP_011537602.1:p.Cys828Ser
|
|
XM_011539301.1:c.2057G>C
|
XP_011537603.1:p.Cys686Ser
|
|
XM_011539302.1:c.2057G>C
|
XP_011537604.1:p.Cys686Ser
|
|
XM_011539308.1:c.*63G>C
|
XP_011537610.1:n.*63G>C
|
|
XM_011539309.1:c.1553G>C
|
XP_011537611.1:p.Cys518Ser
|
|
NM_080722.4:c.2984G>C
MANE Select
|
NP_542453.2:p.Cys995Ser
|
|
NM_139155.3:c.2993G>C
|
NP_631894.2:p.Cys998Ser
|
|
XM_011539300.2:c.2483G>C
|
XP_011537602.1:p.Cys828Ser
|
|
XM_011539301.2:c.2057G>C
|
XP_011537603.1:p.Cys686Ser
|
|
XM_011539302.2:c.2057G>C
|
XP_011537604.1:p.Cys686Ser
|
|
XM_011539308.2:c.*63G>C
|
XP_011537610.1:n.*63G>C
|
|