ENST00000350026.11:c.3976C>T
|
ENSP00000055163.8:p.Pro1326Ser
|
|
ENST00000414678.8:c.4045C>T
|
ENSP00000412835.3:p.Pro1349Ser
|
|
ENST00000637015.2:c.4264C>T
|
ENSP00000489729.2:p.Pro1422Ser
|
|
ENST00000346085.10:c.4015C>T
|
ENSP00000344546.5:p.Pro1339Ser
|
|
ENST00000350026.10:c.3727C>T
|
ENSP00000055163.7:p.Pro1243Ser
|
|
ENST00000414678.7:c.2293C>T
|
ENSP00000412835.2:p.Pro765Ser
|
|
ENST00000635849.1:c.1456C>T
|
ENSP00000490948.1:p.Pro486Ser
|
|
ENST00000635957.1:c.1087C>T
|
ENSP00000490385.1:p.Pro363Ser
|
|
ENST00000636930.2:c.4135C>T
MANE Select
|
ENSP00000490491.2:p.Pro1379Ser
|
|
ENST00000636940.1:n.2132C>T
|
|
|
ENST00000637015.1:c.1503C>T
|
|
|
ENST00000637568.1:c.1417C>T
|
|
|
ENST00000637741.1:n.801C>T
|
|
|
ENST00000637810.1:c.1477C>T
|
ENSP00000489636.1:p.Pro493Ser
|
|
ENST00000637904.1:c.1636C>T
|
ENSP00000490550.1:p.Pro546Ser
|
|
ENST00000647938.1:c.3766C>T
|
ENSP00000498155.1:p.Pro1256Ser
|
|
ENST00000346085.9:c.3766C>T
|
ENSP00000344546.4:p.Pro1256Ser
|
|
ENST00000350026.9:c.3727C>T
|
ENSP00000055163.7:p.Pro1243Ser
|
|
ENST00000414678.6:c.2293C>T
|
ENSP00000412835.2:p.Pro765Ser
|
|
NM_017519.2:c.3727C>T
|
NP_059989.2:p.Pro1243Ser
|
|
NM_020732.3:c.3766C>T
|
NP_065783.3:p.Pro1256Ser
|
|
XM_005267069.3:c.3886C>T
|
XP_005267126.2:p.Pro1296Ser
|
|
XM_011535984.1:c.2965C>T
|
XP_011534286.1:p.Pro989Ser
|
|
XM_011535985.1:c.2785C>T
|
XP_011534287.1:p.Pro929Ser
|
|
XM_011535986.1:c.2545C>T
|
XP_011534288.1:p.Pro849Ser
|
|
XM_011535987.1:c.2164C>T
|
XP_011534289.1:p.Pro722Ser
|
|
XM_011535988.1:c.1027C>T
|
XP_011534290.1:p.Pro343Ser
|
|
NM_001346813.1:c.3886C>T
|
NP_001333742.1:p.Pro1296Ser
|
|
NM_001363725.1:c.1636C>T
|
NP_001350654.1:p.Pro546Ser
|
|
XM_011535984.2:c.4096C>T
|
XP_011534286.2:p.Pro1366Ser
|
|
XM_011535988.3:c.1027C>T
|
XP_011534290.1:p.Pro343Ser
|
|
XM_017011103.2:c.3997C>T
|
XP_016866592.1:p.Pro1333Ser
|
|
XM_017011104.1:c.3967C>T
|
XP_016866593.1:p.Pro1323Ser
|
|
XM_017011105.2:c.3937C>T
|
XP_016866594.1:p.Pro1313Ser
|
|
XM_017011106.2:c.3808C>T
|
XP_016866595.1:p.Pro1270Ser
|
|
XM_017011107.2:c.3787C>T
|
XP_016866596.1:p.Pro1263Ser
|
|
XR_002956289.1:n.4179C>T
|
|
|
NM_001363725.2:c.1636C>T
|
NP_001350654.1:p.Pro546Ser
|
|
NM_001371656.1:c.4015C>T
|
NP_001358585.1:p.Pro1339Ser
|
|
NM_001374820.1:c.4015C>T
|
NP_001361749.1:p.Pro1339Ser
|
|
NM_001374828.1:c.4135C>T
MANE Select
|
NP_001361757.1:p.Pro1379Ser
|
|
NM_017519.3:c.3976C>T
|
NP_059989.3:p.Pro1326Ser
|
|