ENST00000350026.11:c.4651C>A
|
ENSP00000055163.8:p.Pro1551Thr
|
|
ENST00000414678.8:c.4720C>A
|
ENSP00000412835.3:p.Pro1574Thr
|
|
ENST00000637015.2:c.4939C>A
|
ENSP00000489729.2:p.Pro1647Thr
|
|
ENST00000346085.10:c.4690C>A
|
ENSP00000344546.5:p.Pro1564Thr
|
|
ENST00000350026.10:c.4402C>A
|
ENSP00000055163.7:p.Pro1468Thr
|
|
ENST00000414678.7:c.2968C>A
|
ENSP00000412835.2:p.Pro990Thr
|
|
ENST00000635849.1:c.2131C>A
|
ENSP00000490948.1:p.Pro711Thr
|
|
ENST00000635957.1:c.1762C>A
|
ENSP00000490385.1:p.Pro588Thr
|
|
ENST00000636227.1:n.3273C>A
|
|
|
ENST00000636254.1:n.730C>A
|
|
|
ENST00000636930.2:c.4810C>A
MANE Select
|
ENSP00000490491.2:p.Pro1604Thr
|
|
ENST00000636940.1:n.2807C>A
|
|
|
ENST00000637015.1:c.2178C>A
|
|
|
ENST00000637568.1:c.2092C>A
|
|
|
ENST00000637741.1:n.1476C>A
|
|
|
ENST00000637810.1:c.2152C>A
|
ENSP00000489636.1:p.Pro718Thr
|
|
ENST00000637904.1:c.2311C>A
|
ENSP00000490550.1:p.Pro771Thr
|
|
ENST00000647938.1:c.4441C>A
|
ENSP00000498155.1:p.Pro1481Thr
|
|
ENST00000346085.9:c.4441C>A
|
ENSP00000344546.4:p.Pro1481Thr
|
|
ENST00000350026.9:c.4402C>A
|
ENSP00000055163.7:p.Pro1468Thr
|
|
ENST00000414678.6:c.2968C>A
|
ENSP00000412835.2:p.Pro990Thr
|
|
NM_017519.2:c.4402C>A
|
NP_059989.2:p.Pro1468Thr
|
|
NM_020732.3:c.4441C>A
|
NP_065783.3:p.Pro1481Thr
|
|
XM_005267069.3:c.4561C>A
|
XP_005267126.2:p.Pro1521Thr
|
|
XM_011535984.1:c.3640C>A
|
XP_011534286.1:p.Pro1214Thr
|
|
XM_011535985.1:c.3460C>A
|
XP_011534287.1:p.Pro1154Thr
|
|
XM_011535986.1:c.3220C>A
|
XP_011534288.1:p.Pro1074Thr
|
|
XM_011535987.1:c.2839C>A
|
XP_011534289.1:p.Pro947Thr
|
|
XM_011535988.1:c.1702C>A
|
XP_011534290.1:p.Pro568Thr
|
|
NM_001346813.1:c.4561C>A
|
NP_001333742.1:p.Pro1521Thr
|
|
NM_001363725.1:c.2311C>A
|
NP_001350654.1:p.Pro771Thr
|
|
XM_011535984.2:c.4771C>A
|
XP_011534286.2:p.Pro1591Thr
|
|
XM_011535988.3:c.1702C>A
|
XP_011534290.1:p.Pro568Thr
|
|
XM_017011103.2:c.4672C>A
|
XP_016866592.1:p.Pro1558Thr
|
|
XM_017011104.1:c.4642C>A
|
XP_016866593.1:p.Pro1548Thr
|
|
XM_017011105.2:c.4612C>A
|
XP_016866594.1:p.Pro1538Thr
|
|
XM_017011106.2:c.4483C>A
|
XP_016866595.1:p.Pro1495Thr
|
|
XM_017011107.2:c.4462C>A
|
XP_016866596.1:p.Pro1488Thr
|
|
XR_002956289.1:n.4757C>A
|
|
|
NM_001363725.2:c.2311C>A
|
NP_001350654.1:p.Pro771Thr
|
|
NM_001371656.1:c.4690C>A
|
NP_001358585.1:p.Pro1564Thr
|
|
NM_001374820.1:c.4690C>A
|
NP_001361749.1:p.Pro1564Thr
|
|
NM_001374828.1:c.4810C>A
MANE Select
|
NP_001361757.1:p.Pro1604Thr
|
|
NM_017519.3:c.4651C>A
|
NP_059989.3:p.Pro1551Thr
|
|