ENST00000350026.11:c.4672C>T
|
ENSP00000055163.8:p.Pro1558Ser
|
|
ENST00000414678.8:c.4741C>T
|
ENSP00000412835.3:p.Pro1581Ser
|
|
ENST00000637015.2:c.4960C>T
|
ENSP00000489729.2:p.Pro1654Ser
|
|
ENST00000346085.10:c.4711C>T
|
ENSP00000344546.5:p.Pro1571Ser
|
|
ENST00000350026.10:c.4423C>T
|
ENSP00000055163.7:p.Pro1475Ser
|
|
ENST00000414678.7:c.2989C>T
|
ENSP00000412835.2:p.Pro997Ser
|
|
ENST00000635849.1:c.2152C>T
|
ENSP00000490948.1:p.Pro718Ser
|
|
ENST00000635957.1:c.1783C>T
|
ENSP00000490385.1:p.Pro595Ser
|
|
ENST00000636227.1:n.3294C>T
|
|
|
ENST00000636254.1:n.751C>T
|
|
|
ENST00000636930.2:c.4831C>T
MANE Select
|
ENSP00000490491.2:p.Pro1611Ser
|
|
ENST00000636940.1:n.2828C>T
|
|
|
ENST00000637015.1:c.2199C>T
|
|
|
ENST00000637568.1:c.2113C>T
|
|
|
ENST00000637741.1:n.1497C>T
|
|
|
ENST00000637810.1:c.2173C>T
|
ENSP00000489636.1:p.Pro725Ser
|
|
ENST00000637904.1:c.2332C>T
|
ENSP00000490550.1:p.Pro778Ser
|
|
ENST00000647938.1:c.4462C>T
|
ENSP00000498155.1:p.Pro1488Ser
|
|
ENST00000346085.9:c.4462C>T
|
ENSP00000344546.4:p.Pro1488Ser
|
|
ENST00000350026.9:c.4423C>T
|
ENSP00000055163.7:p.Pro1475Ser
|
|
ENST00000414678.6:c.2989C>T
|
ENSP00000412835.2:p.Pro997Ser
|
|
NM_017519.2:c.4423C>T
|
NP_059989.2:p.Pro1475Ser
|
|
NM_020732.3:c.4462C>T
|
NP_065783.3:p.Pro1488Ser
|
|
XM_005267069.3:c.4582C>T
|
XP_005267126.2:p.Pro1528Ser
|
|
XM_011535984.1:c.3661C>T
|
XP_011534286.1:p.Pro1221Ser
|
|
XM_011535985.1:c.3481C>T
|
XP_011534287.1:p.Pro1161Ser
|
|
XM_011535986.1:c.3241C>T
|
XP_011534288.1:p.Pro1081Ser
|
|
XM_011535987.1:c.2860C>T
|
XP_011534289.1:p.Pro954Ser
|
|
XM_011535988.1:c.1723C>T
|
XP_011534290.1:p.Pro575Ser
|
|
NM_001346813.1:c.4582C>T
|
NP_001333742.1:p.Pro1528Ser
|
|
NM_001363725.1:c.2332C>T
|
NP_001350654.1:p.Pro778Ser
|
|
XM_011535984.2:c.4792C>T
|
XP_011534286.2:p.Pro1598Ser
|
|
XM_011535988.3:c.1723C>T
|
XP_011534290.1:p.Pro575Ser
|
|
XM_017011103.2:c.4693C>T
|
XP_016866592.1:p.Pro1565Ser
|
|
XM_017011104.1:c.4663C>T
|
XP_016866593.1:p.Pro1555Ser
|
|
XM_017011105.2:c.4633C>T
|
XP_016866594.1:p.Pro1545Ser
|
|
XM_017011106.2:c.4504C>T
|
XP_016866595.1:p.Pro1502Ser
|
|
XM_017011107.2:c.4483C>T
|
XP_016866596.1:p.Pro1495Ser
|
|
XR_002956289.1:n.4778C>T
|
|
|
NM_001363725.2:c.2332C>T
|
NP_001350654.1:p.Pro778Ser
|
|
NM_001371656.1:c.4711C>T
|
NP_001358585.1:p.Pro1571Ser
|
|
NM_001374820.1:c.4711C>T
|
NP_001361749.1:p.Pro1571Ser
|
|
NM_001374828.1:c.4831C>T
MANE Select
|
NP_001361757.1:p.Pro1611Ser
|
|
NM_017519.3:c.4672C>T
|
NP_059989.3:p.Pro1558Ser
|
|