ENST00000350026.11:c.2932C>A
|
ENSP00000055163.8:p.Pro978Thr
|
|
ENST00000414678.8:c.2842C>A
|
ENSP00000412835.3:p.Pro948Thr
|
|
ENST00000637015.2:c.2932C>A
|
ENSP00000489729.2:p.Pro978Thr
|
|
ENST00000319584.11:c.946C>A
|
ENSP00000313006.7:p.Pro316Thr
|
|
ENST00000346085.10:c.2971C>A
|
ENSP00000344546.5:p.Pro991Thr
|
|
ENST00000350026.10:c.2683C>A
|
ENSP00000055163.7:p.Pro895Thr
|
|
ENST00000414678.7:c.1090C>A
|
ENSP00000412835.2:p.Pro364Thr
|
|
ENST00000452544.2:n.833C>A
|
|
|
ENST00000635849.1:c.253C>A
|
ENSP00000490948.1:p.Pro85Thr
|
|
ENST00000636426.1:n.66C>A
|
|
|
ENST00000636930.2:c.2932C>A
MANE Select
|
ENSP00000490491.2:p.Pro978Thr
|
|
ENST00000637015.1:c.171C>A
|
|
|
ENST00000637810.1:c.433C>A
|
ENSP00000489636.1:p.Pro145Thr
|
|
ENST00000637904.1:c.433C>A
|
ENSP00000490550.1:p.Pro145Thr
|
|
ENST00000647938.1:c.2722C>A
|
ENSP00000498155.1:p.Pro908Thr
|
|
ENST00000674190.1:n.1681C>A
|
|
|
ENST00000319584.10:c.949C>A
|
ENSP00000313006.6:p.Pro317Thr
|
|
ENST00000346085.9:c.2722C>A
|
ENSP00000344546.4:p.Pro908Thr
|
|
ENST00000350026.9:c.2683C>A
|
ENSP00000055163.7:p.Pro895Thr
|
|
ENST00000414678.6:c.1090C>A
|
ENSP00000412835.2:p.Pro364Thr
|
|
ENST00000452544.1:n.779C>A
|
|
|
ENST00000478761.3:c.5C>A
|
|
|
NM_017519.2:c.2683C>A
|
NP_059989.2:p.Pro895Thr
|
|
NM_020732.3:c.2722C>A
|
NP_065783.3:p.Pro908Thr
|
|
XM_005267069.3:c.2683C>A
|
XP_005267126.2:p.Pro895Thr
|
|
XM_011535984.1:c.1633C>A
|
XP_011534286.1:p.Pro545Thr
|
|
XM_011535985.1:c.1453C>A
|
XP_011534287.1:p.Pro485Thr
|
|
XM_011535986.1:c.1213C>A
|
XP_011534288.1:p.Pro405Thr
|
|
XM_011535987.1:c.832C>A
|
XP_011534289.1:p.Pro278Thr
|
|
XM_011535988.1:c.-20+15587C>A
|
XP_011534290.1:n.-20+15587C>A
|
|
NM_001346813.1:c.2683C>A
|
NP_001333742.1:p.Pro895Thr
|
|
NM_001363725.1:c.433C>A
|
NP_001350654.1:p.Pro145Thr
|
|
XM_011535984.2:c.2764C>A
|
XP_011534286.2:p.Pro922Thr
|
|
XM_011535988.3:c.-20+15587C>A
|
XP_011534290.1:n.-20+15587C>A
|
|
XM_017011103.2:c.2764C>A
|
XP_016866592.1:p.Pro922Thr
|
|
XM_017011104.1:c.2764C>A
|
XP_016866593.1:p.Pro922Thr
|
|
XM_017011105.2:c.2764C>A
|
XP_016866594.1:p.Pro922Thr
|
|
XM_017011106.2:c.2764C>A
|
XP_016866595.1:p.Pro922Thr
|
|
XM_017011107.2:c.2584C>A
|
XP_016866596.1:p.Pro862Thr
|
|
XR_002956289.1:n.2847C>A
|
|
|
NM_001363725.2:c.433C>A
|
NP_001350654.1:p.Pro145Thr
|
|
NM_001371656.1:c.2971C>A
|
NP_001358585.1:p.Pro991Thr
|
|
NM_001374820.1:c.2971C>A
|
NP_001361749.1:p.Pro991Thr
|
|
NM_001374828.1:c.2932C>A
MANE Select
|
NP_001361757.1:p.Pro978Thr
|
|
NM_017519.3:c.2932C>A
|
NP_059989.3:p.Pro978Thr
|
|