ENST00000350026.11:c.4653T>G
|
ENSP00000055163.8:p.Pro1551=
|
|
ENST00000414678.8:c.4722T>G
|
ENSP00000412835.3:p.Pro1574=
|
|
ENST00000637015.2:c.4941T>G
|
ENSP00000489729.2:p.Pro1647=
|
|
ENST00000346085.10:c.4692T>G
|
ENSP00000344546.5:p.Pro1564=
|
|
ENST00000350026.10:c.4404T>G
|
ENSP00000055163.7:p.Pro1468=
|
|
ENST00000414678.7:c.2970T>G
|
ENSP00000412835.2:p.Pro990=
|
|
ENST00000635849.1:c.2133T>G
|
ENSP00000490948.1:p.Pro711=
|
|
ENST00000635957.1:c.1764T>G
|
ENSP00000490385.1:p.Pro588=
|
|
ENST00000636227.1:n.3275T>G
|
|
|
ENST00000636254.1:n.732T>G
|
|
|
ENST00000636930.2:c.4812T>G
MANE Select
|
ENSP00000490491.2:p.Pro1604=
|
|
ENST00000636940.1:n.2809T>G
|
|
|
ENST00000637015.1:c.2180T>G
|
|
|
ENST00000637568.1:c.2094T>G
|
|
|
ENST00000637741.1:n.1478T>G
|
|
|
ENST00000637810.1:c.2154T>G
|
ENSP00000489636.1:p.Pro718=
|
|
ENST00000637904.1:c.2313T>G
|
ENSP00000490550.1:p.Pro771=
|
|
ENST00000647938.1:c.4443T>G
|
ENSP00000498155.1:p.Pro1481=
|
|
ENST00000346085.9:c.4443T>G
|
ENSP00000344546.4:p.Pro1481=
|
|
ENST00000350026.9:c.4404T>G
|
ENSP00000055163.7:p.Pro1468=
|
|
ENST00000414678.6:c.2970T>G
|
ENSP00000412835.2:p.Pro990=
|
|
NM_017519.2:c.4404T>G
|
NP_059989.2:p.Pro1468=
|
|
NM_020732.3:c.4443T>G
|
NP_065783.3:p.Pro1481=
|
|
XM_005267069.3:c.4563T>G
|
XP_005267126.2:p.Pro1521=
|
|
XM_011535984.1:c.3642T>G
|
XP_011534286.1:p.Pro1214=
|
|
XM_011535985.1:c.3462T>G
|
XP_011534287.1:p.Pro1154=
|
|
XM_011535986.1:c.3222T>G
|
XP_011534288.1:p.Pro1074=
|
|
XM_011535987.1:c.2841T>G
|
XP_011534289.1:p.Pro947=
|
|
XM_011535988.1:c.1704T>G
|
XP_011534290.1:p.Pro568=
|
|
NM_001346813.1:c.4563T>G
|
NP_001333742.1:p.Pro1521=
|
|
NM_001363725.1:c.2313T>G
|
NP_001350654.1:p.Pro771=
|
|
XM_011535984.2:c.4773T>G
|
XP_011534286.2:p.Pro1591=
|
|
XM_011535988.3:c.1704T>G
|
XP_011534290.1:p.Pro568=
|
|
XM_017011103.2:c.4674T>G
|
XP_016866592.1:p.Pro1558=
|
|
XM_017011104.1:c.4644T>G
|
XP_016866593.1:p.Pro1548=
|
|
XM_017011105.2:c.4614T>G
|
XP_016866594.1:p.Pro1538=
|
|
XM_017011106.2:c.4485T>G
|
XP_016866595.1:p.Pro1495=
|
|
XM_017011107.2:c.4464T>G
|
XP_016866596.1:p.Pro1488=
|
|
XR_002956289.1:n.4759T>G
|
|
|
NM_001363725.2:c.2313T>G
|
NP_001350654.1:p.Pro771=
|
|
NM_001371656.1:c.4692T>G
|
NP_001358585.1:p.Pro1564=
|
|
NM_001374820.1:c.4692T>G
|
NP_001361749.1:p.Pro1564=
|
|
NM_001374828.1:c.4812T>G
MANE Select
|
NP_001361757.1:p.Pro1604=
|
|
NM_017519.3:c.4653T>G
|
NP_059989.3:p.Pro1551=
|
|