ENST00000350026.11:c.3883C>A
|
ENSP00000055163.8:p.Pro1295Thr
|
|
ENST00000414678.8:c.3952C>A
|
ENSP00000412835.3:p.Pro1318Thr
|
|
ENST00000637015.2:c.4171C>A
|
ENSP00000489729.2:p.Pro1391Thr
|
|
ENST00000346085.10:c.3922C>A
|
ENSP00000344546.5:p.Pro1308Thr
|
|
ENST00000350026.10:c.3634C>A
|
ENSP00000055163.7:p.Pro1212Thr
|
|
ENST00000414678.7:c.2200C>A
|
ENSP00000412835.2:p.Pro734Thr
|
|
ENST00000635849.1:c.1363C>A
|
ENSP00000490948.1:p.Pro455Thr
|
|
ENST00000635957.1:c.997C>A
|
ENSP00000490385.1:p.Pro333Thr
|
|
ENST00000636930.2:c.4042C>A
MANE Select
|
ENSP00000490491.2:p.Pro1348Thr
|
|
ENST00000636940.1:n.2039C>A
|
|
|
ENST00000637015.1:c.1410C>A
|
|
|
ENST00000637568.1:c.1324C>A
|
|
|
ENST00000637741.1:n.708C>A
|
|
|
ENST00000637810.1:c.1384C>A
|
ENSP00000489636.1:p.Pro462Thr
|
|
ENST00000637904.1:c.1543C>A
|
ENSP00000490550.1:p.Pro515Thr
|
|
ENST00000647938.1:c.3673C>A
|
ENSP00000498155.1:p.Pro1225Thr
|
|
ENST00000346085.9:c.3673C>A
|
ENSP00000344546.4:p.Pro1225Thr
|
|
ENST00000350026.9:c.3634C>A
|
ENSP00000055163.7:p.Pro1212Thr
|
|
ENST00000414678.6:c.2200C>A
|
ENSP00000412835.2:p.Pro734Thr
|
|
NM_017519.2:c.3634C>A
|
NP_059989.2:p.Pro1212Thr
|
|
NM_020732.3:c.3673C>A
|
NP_065783.3:p.Pro1225Thr
|
|
XM_005267069.3:c.3793C>A
|
XP_005267126.2:p.Pro1265Thr
|
|
XM_011535984.1:c.2872C>A
|
XP_011534286.1:p.Pro958Thr
|
|
XM_011535985.1:c.2692C>A
|
XP_011534287.1:p.Pro898Thr
|
|
XM_011535986.1:c.2452C>A
|
XP_011534288.1:p.Pro818Thr
|
|
XM_011535987.1:c.2071C>A
|
XP_011534289.1:p.Pro691Thr
|
|
XM_011535988.1:c.934C>A
|
XP_011534290.1:p.Pro312Thr
|
|
NM_001346813.1:c.3793C>A
|
NP_001333742.1:p.Pro1265Thr
|
|
NM_001363725.1:c.1543C>A
|
NP_001350654.1:p.Pro515Thr
|
|
XM_011535984.2:c.4003C>A
|
XP_011534286.2:p.Pro1335Thr
|
|
XM_011535988.3:c.934C>A
|
XP_011534290.1:p.Pro312Thr
|
|
XM_017011103.2:c.3904C>A
|
XP_016866592.1:p.Pro1302Thr
|
|
XM_017011104.1:c.3874C>A
|
XP_016866593.1:p.Pro1292Thr
|
|
XM_017011105.2:c.3844C>A
|
XP_016866594.1:p.Pro1282Thr
|
|
XM_017011106.2:c.3715C>A
|
XP_016866595.1:p.Pro1239Thr
|
|
XM_017011107.2:c.3694C>A
|
XP_016866596.1:p.Pro1232Thr
|
|
XR_002956289.1:n.4086C>A
|
|
|
NM_001363725.2:c.1543C>A
|
NP_001350654.1:p.Pro515Thr
|
|
NM_001371656.1:c.3922C>A
|
NP_001358585.1:p.Pro1308Thr
|
|
NM_001374820.1:c.3922C>A
|
NP_001361749.1:p.Pro1308Thr
|
|
NM_001374828.1:c.4042C>A
MANE Select
|
NP_001361757.1:p.Pro1348Thr
|
|
NM_017519.3:c.3883C>A
|
NP_059989.3:p.Pro1295Thr
|
|