ENST00000350026.11:c.4822C>A
|
ENSP00000055163.8:p.Pro1608Thr
|
|
ENST00000414678.8:c.4891C>A
|
ENSP00000412835.3:p.Pro1631Thr
|
|
ENST00000637015.2:c.5110C>A
|
ENSP00000489729.2:p.Pro1704Thr
|
|
ENST00000346085.10:c.4861C>A
|
ENSP00000344546.5:p.Pro1621Thr
|
|
ENST00000350026.10:c.4573C>A
|
ENSP00000055163.7:p.Pro1525Thr
|
|
ENST00000414678.7:c.3139C>A
|
ENSP00000412835.2:p.Pro1047Thr
|
|
ENST00000635849.1:c.2302C>A
|
ENSP00000490948.1:p.Pro768Thr
|
|
ENST00000635957.1:c.1933C>A
|
ENSP00000490385.1:p.Pro645Thr
|
|
ENST00000636227.1:n.3444C>A
|
|
|
ENST00000636254.1:n.901C>A
|
|
|
ENST00000636930.2:c.4981C>A
MANE Select
|
ENSP00000490491.2:p.Pro1661Thr
|
|
ENST00000636940.1:n.2978C>A
|
|
|
ENST00000637015.1:c.2349C>A
|
|
|
ENST00000637568.1:c.2263C>A
|
|
|
ENST00000637741.1:n.1647C>A
|
|
|
ENST00000637810.1:c.2323C>A
|
ENSP00000489636.1:p.Pro775Thr
|
|
ENST00000637904.1:c.2482C>A
|
ENSP00000490550.1:p.Pro828Thr
|
|
ENST00000647938.1:c.4612C>A
|
ENSP00000498155.1:p.Pro1538Thr
|
|
ENST00000346085.9:c.4612C>A
|
ENSP00000344546.4:p.Pro1538Thr
|
|
ENST00000350026.9:c.4573C>A
|
ENSP00000055163.7:p.Pro1525Thr
|
|
ENST00000414678.6:c.3139C>A
|
ENSP00000412835.2:p.Pro1047Thr
|
|
NM_017519.2:c.4573C>A
|
NP_059989.2:p.Pro1525Thr
|
|
NM_020732.3:c.4612C>A
|
NP_065783.3:p.Pro1538Thr
|
|
XM_005267069.3:c.4732C>A
|
XP_005267126.2:p.Pro1578Thr
|
|
XM_011535984.1:c.3811C>A
|
XP_011534286.1:p.Pro1271Thr
|
|
XM_011535985.1:c.3631C>A
|
XP_011534287.1:p.Pro1211Thr
|
|
XM_011535986.1:c.3391C>A
|
XP_011534288.1:p.Pro1131Thr
|
|
XM_011535987.1:c.3010C>A
|
XP_011534289.1:p.Pro1004Thr
|
|
XM_011535988.1:c.1873C>A
|
XP_011534290.1:p.Pro625Thr
|
|
NM_001346813.1:c.4732C>A
|
NP_001333742.1:p.Pro1578Thr
|
|
NM_001363725.1:c.2482C>A
|
NP_001350654.1:p.Pro828Thr
|
|
XM_011535984.2:c.4942C>A
|
XP_011534286.2:p.Pro1648Thr
|
|
XM_011535988.3:c.1873C>A
|
XP_011534290.1:p.Pro625Thr
|
|
XM_017011103.2:c.4843C>A
|
XP_016866592.1:p.Pro1615Thr
|
|
XM_017011104.1:c.4813C>A
|
XP_016866593.1:p.Pro1605Thr
|
|
XM_017011105.2:c.4783C>A
|
XP_016866594.1:p.Pro1595Thr
|
|
XM_017011106.2:c.4654C>A
|
XP_016866595.1:p.Pro1552Thr
|
|
XM_017011107.2:c.4633C>A
|
XP_016866596.1:p.Pro1545Thr
|
|
XR_002956289.1:n.4928C>A
|
|
|
NM_001363725.2:c.2482C>A
|
NP_001350654.1:p.Pro828Thr
|
|
NM_001371656.1:c.4861C>A
|
NP_001358585.1:p.Pro1621Thr
|
|
NM_001374820.1:c.4861C>A
|
NP_001361749.1:p.Pro1621Thr
|
|
NM_001374828.1:c.4981C>A
MANE Select
|
NP_001361757.1:p.Pro1661Thr
|
|
NM_017519.3:c.4822C>A
|
NP_059989.3:p.Pro1608Thr
|
|