ENST00000350026.11:c.2796G>C
|
ENSP00000055163.8:p.Val932=
|
|
ENST00000414678.8:c.2706G>C
|
ENSP00000412835.3:p.Val902=
|
|
ENST00000637015.2:c.2796G>C
|
ENSP00000489729.2:p.Val932=
|
|
ENST00000319584.11:c.810G>C
|
ENSP00000313006.7:p.Val270=
|
|
ENST00000346085.10:c.2835G>C
|
ENSP00000344546.5:p.Val945=
|
|
ENST00000350026.10:c.2547G>C
|
ENSP00000055163.7:p.Val849=
|
|
ENST00000414678.7:c.954G>C
|
ENSP00000412835.2:p.Val318=
|
|
ENST00000452544.2:n.697G>C
|
|
|
ENST00000635849.1:c.117G>C
|
ENSP00000490948.1:p.Val39=
|
|
ENST00000636930.2:c.2796G>C
MANE Select
|
ENSP00000490491.2:p.Val932=
|
|
ENST00000637015.1:c.35G>C
|
|
|
ENST00000637810.1:c.297G>C
|
ENSP00000489636.1:p.Val99=
|
|
ENST00000637904.1:c.297G>C
|
ENSP00000490550.1:p.Val99=
|
|
ENST00000647938.1:c.2586G>C
|
ENSP00000498155.1:p.Val862=
|
|
ENST00000674190.1:n.1545G>C
|
|
|
ENST00000319584.10:c.813G>C
|
ENSP00000313006.6:p.Val271=
|
|
ENST00000346085.9:c.2586G>C
|
ENSP00000344546.4:p.Val862=
|
|
ENST00000350026.9:c.2547G>C
|
ENSP00000055163.7:p.Val849=
|
|
ENST00000414678.6:c.954G>C
|
ENSP00000412835.2:p.Val318=
|
|
ENST00000452544.1:n.643G>C
|
|
|
NM_017519.2:c.2547G>C
|
NP_059989.2:p.Val849=
|
|
NM_020732.3:c.2586G>C
|
NP_065783.3:p.Val862=
|
|
XM_005267069.3:c.2547G>C
|
XP_005267126.2:p.Val849=
|
|
XM_011535984.1:c.1497G>C
|
XP_011534286.1:p.Val499=
|
|
XM_011535985.1:c.1317G>C
|
XP_011534287.1:p.Val439=
|
|
XM_011535986.1:c.1077G>C
|
XP_011534288.1:p.Val359=
|
|
XM_011535987.1:c.696G>C
|
XP_011534289.1:p.Val232=
|
|
XM_011535988.1:c.-20+15451G>C
|
XP_011534290.1:n.-20+15451G>C
|
|
NM_001346813.1:c.2547G>C
|
NP_001333742.1:p.Val849=
|
|
NM_001363725.1:c.297G>C
|
NP_001350654.1:p.Val99=
|
|
XM_011535984.2:c.2628G>C
|
XP_011534286.2:p.Val876=
|
|
XM_011535988.3:c.-20+15451G>C
|
XP_011534290.1:n.-20+15451G>C
|
|
XM_017011103.2:c.2628G>C
|
XP_016866592.1:p.Val876=
|
|
XM_017011104.1:c.2628G>C
|
XP_016866593.1:p.Val876=
|
|
XM_017011105.2:c.2628G>C
|
XP_016866594.1:p.Val876=
|
|
XM_017011106.2:c.2628G>C
|
XP_016866595.1:p.Val876=
|
|
XM_017011107.2:c.2448G>C
|
XP_016866596.1:p.Val816=
|
|
XR_002956289.1:n.2711G>C
|
|
|
NM_001363725.2:c.297G>C
|
NP_001350654.1:p.Val99=
|
|
NM_001371656.1:c.2835G>C
|
NP_001358585.1:p.Val945=
|
|
NM_001374820.1:c.2835G>C
|
NP_001361749.1:p.Val945=
|
|
NM_001374828.1:c.2796G>C
MANE Select
|
NP_001361757.1:p.Val932=
|
|
NM_017519.3:c.2796G>C
|
NP_059989.3:p.Val932=
|
|