ENST00000350026.11:c.3976C>A
|
ENSP00000055163.8:p.Pro1326Thr
|
|
ENST00000414678.8:c.4045C>A
|
ENSP00000412835.3:p.Pro1349Thr
|
|
ENST00000637015.2:c.4264C>A
|
ENSP00000489729.2:p.Pro1422Thr
|
|
ENST00000346085.10:c.4015C>A
|
ENSP00000344546.5:p.Pro1339Thr
|
|
ENST00000350026.10:c.3727C>A
|
ENSP00000055163.7:p.Pro1243Thr
|
|
ENST00000414678.7:c.2293C>A
|
ENSP00000412835.2:p.Pro765Thr
|
|
ENST00000635849.1:c.1456C>A
|
ENSP00000490948.1:p.Pro486Thr
|
|
ENST00000635957.1:c.1087C>A
|
ENSP00000490385.1:p.Pro363Thr
|
|
ENST00000636930.2:c.4135C>A
MANE Select
|
ENSP00000490491.2:p.Pro1379Thr
|
|
ENST00000636940.1:n.2132C>A
|
|
|
ENST00000637015.1:c.1503C>A
|
|
|
ENST00000637568.1:c.1417C>A
|
|
|
ENST00000637741.1:n.801C>A
|
|
|
ENST00000637810.1:c.1477C>A
|
ENSP00000489636.1:p.Pro493Thr
|
|
ENST00000637904.1:c.1636C>A
|
ENSP00000490550.1:p.Pro546Thr
|
|
ENST00000647938.1:c.3766C>A
|
ENSP00000498155.1:p.Pro1256Thr
|
|
ENST00000346085.9:c.3766C>A
|
ENSP00000344546.4:p.Pro1256Thr
|
|
ENST00000350026.9:c.3727C>A
|
ENSP00000055163.7:p.Pro1243Thr
|
|
ENST00000414678.6:c.2293C>A
|
ENSP00000412835.2:p.Pro765Thr
|
|
NM_017519.2:c.3727C>A
|
NP_059989.2:p.Pro1243Thr
|
|
NM_020732.3:c.3766C>A
|
NP_065783.3:p.Pro1256Thr
|
|
XM_005267069.3:c.3886C>A
|
XP_005267126.2:p.Pro1296Thr
|
|
XM_011535984.1:c.2965C>A
|
XP_011534286.1:p.Pro989Thr
|
|
XM_011535985.1:c.2785C>A
|
XP_011534287.1:p.Pro929Thr
|
|
XM_011535986.1:c.2545C>A
|
XP_011534288.1:p.Pro849Thr
|
|
XM_011535987.1:c.2164C>A
|
XP_011534289.1:p.Pro722Thr
|
|
XM_011535988.1:c.1027C>A
|
XP_011534290.1:p.Pro343Thr
|
|
NM_001346813.1:c.3886C>A
|
NP_001333742.1:p.Pro1296Thr
|
|
NM_001363725.1:c.1636C>A
|
NP_001350654.1:p.Pro546Thr
|
|
XM_011535984.2:c.4096C>A
|
XP_011534286.2:p.Pro1366Thr
|
|
XM_011535988.3:c.1027C>A
|
XP_011534290.1:p.Pro343Thr
|
|
XM_017011103.2:c.3997C>A
|
XP_016866592.1:p.Pro1333Thr
|
|
XM_017011104.1:c.3967C>A
|
XP_016866593.1:p.Pro1323Thr
|
|
XM_017011105.2:c.3937C>A
|
XP_016866594.1:p.Pro1313Thr
|
|
XM_017011106.2:c.3808C>A
|
XP_016866595.1:p.Pro1270Thr
|
|
XM_017011107.2:c.3787C>A
|
XP_016866596.1:p.Pro1263Thr
|
|
XR_002956289.1:n.4179C>A
|
|
|
NM_001363725.2:c.1636C>A
|
NP_001350654.1:p.Pro546Thr
|
|
NM_001371656.1:c.4015C>A
|
NP_001358585.1:p.Pro1339Thr
|
|
NM_001374820.1:c.4015C>A
|
NP_001361749.1:p.Pro1339Thr
|
|
NM_001374828.1:c.4135C>A
MANE Select
|
NP_001361757.1:p.Pro1379Thr
|
|
NM_017519.3:c.3976C>A
|
NP_059989.3:p.Pro1326Thr
|
|