ENST00000350026.11:c.4675C>A
|
ENSP00000055163.8:p.Pro1559Thr
|
|
ENST00000414678.8:c.4744C>A
|
ENSP00000412835.3:p.Pro1582Thr
|
|
ENST00000637015.2:c.4963C>A
|
ENSP00000489729.2:p.Pro1655Thr
|
|
ENST00000346085.10:c.4714C>A
|
ENSP00000344546.5:p.Pro1572Thr
|
|
ENST00000350026.10:c.4426C>A
|
ENSP00000055163.7:p.Pro1476Thr
|
|
ENST00000414678.7:c.2992C>A
|
ENSP00000412835.2:p.Pro998Thr
|
|
ENST00000635849.1:c.2155C>A
|
ENSP00000490948.1:p.Pro719Thr
|
|
ENST00000635957.1:c.1786C>A
|
ENSP00000490385.1:p.Pro596Thr
|
|
ENST00000636227.1:n.3297C>A
|
|
|
ENST00000636254.1:n.754C>A
|
|
|
ENST00000636930.2:c.4834C>A
MANE Select
|
ENSP00000490491.2:p.Pro1612Thr
|
|
ENST00000636940.1:n.2831C>A
|
|
|
ENST00000637015.1:c.2202C>A
|
|
|
ENST00000637568.1:c.2116C>A
|
|
|
ENST00000637741.1:n.1500C>A
|
|
|
ENST00000637810.1:c.2176C>A
|
ENSP00000489636.1:p.Pro726Thr
|
|
ENST00000637904.1:c.2335C>A
|
ENSP00000490550.1:p.Pro779Thr
|
|
ENST00000647938.1:c.4465C>A
|
ENSP00000498155.1:p.Pro1489Thr
|
|
ENST00000346085.9:c.4465C>A
|
ENSP00000344546.4:p.Pro1489Thr
|
|
ENST00000350026.9:c.4426C>A
|
ENSP00000055163.7:p.Pro1476Thr
|
|
ENST00000414678.6:c.2992C>A
|
ENSP00000412835.2:p.Pro998Thr
|
|
NM_017519.2:c.4426C>A
|
NP_059989.2:p.Pro1476Thr
|
|
NM_020732.3:c.4465C>A
|
NP_065783.3:p.Pro1489Thr
|
|
XM_005267069.3:c.4585C>A
|
XP_005267126.2:p.Pro1529Thr
|
|
XM_011535984.1:c.3664C>A
|
XP_011534286.1:p.Pro1222Thr
|
|
XM_011535985.1:c.3484C>A
|
XP_011534287.1:p.Pro1162Thr
|
|
XM_011535986.1:c.3244C>A
|
XP_011534288.1:p.Pro1082Thr
|
|
XM_011535987.1:c.2863C>A
|
XP_011534289.1:p.Pro955Thr
|
|
XM_011535988.1:c.1726C>A
|
XP_011534290.1:p.Pro576Thr
|
|
NM_001346813.1:c.4585C>A
|
NP_001333742.1:p.Pro1529Thr
|
|
NM_001363725.1:c.2335C>A
|
NP_001350654.1:p.Pro779Thr
|
|
XM_011535984.2:c.4795C>A
|
XP_011534286.2:p.Pro1599Thr
|
|
XM_011535988.3:c.1726C>A
|
XP_011534290.1:p.Pro576Thr
|
|
XM_017011103.2:c.4696C>A
|
XP_016866592.1:p.Pro1566Thr
|
|
XM_017011104.1:c.4666C>A
|
XP_016866593.1:p.Pro1556Thr
|
|
XM_017011105.2:c.4636C>A
|
XP_016866594.1:p.Pro1546Thr
|
|
XM_017011106.2:c.4507C>A
|
XP_016866595.1:p.Pro1503Thr
|
|
XM_017011107.2:c.4486C>A
|
XP_016866596.1:p.Pro1496Thr
|
|
XR_002956289.1:n.4781C>A
|
|
|
NM_001363725.2:c.2335C>A
|
NP_001350654.1:p.Pro779Thr
|
|
NM_001371656.1:c.4714C>A
|
NP_001358585.1:p.Pro1572Thr
|
|
NM_001374820.1:c.4714C>A
|
NP_001361749.1:p.Pro1572Thr
|
|
NM_001374828.1:c.4834C>A
MANE Select
|
NP_001361757.1:p.Pro1612Thr
|
|
NM_017519.3:c.4675C>A
|
NP_059989.3:p.Pro1559Thr
|
|