ENST00000350026.11:c.4624C>A
|
ENSP00000055163.8:p.Pro1542Thr
|
|
ENST00000414678.8:c.4693C>A
|
ENSP00000412835.3:p.Pro1565Thr
|
|
ENST00000637015.2:c.4912C>A
|
ENSP00000489729.2:p.Pro1638Thr
|
|
ENST00000346085.10:c.4663C>A
|
ENSP00000344546.5:p.Pro1555Thr
|
|
ENST00000350026.10:c.4375C>A
|
ENSP00000055163.7:p.Pro1459Thr
|
|
ENST00000414678.7:c.2941C>A
|
ENSP00000412835.2:p.Pro981Thr
|
|
ENST00000635849.1:c.2104C>A
|
ENSP00000490948.1:p.Pro702Thr
|
|
ENST00000635957.1:c.1735C>A
|
ENSP00000490385.1:p.Pro579Thr
|
|
ENST00000636227.1:n.3246C>A
|
|
|
ENST00000636254.1:n.703C>A
|
|
|
ENST00000636930.2:c.4783C>A
MANE Select
|
ENSP00000490491.2:p.Pro1595Thr
|
|
ENST00000636940.1:n.2780C>A
|
|
|
ENST00000637015.1:c.2151C>A
|
|
|
ENST00000637568.1:c.2065C>A
|
|
|
ENST00000637741.1:n.1449C>A
|
|
|
ENST00000637810.1:c.2125C>A
|
ENSP00000489636.1:p.Pro709Thr
|
|
ENST00000637904.1:c.2284C>A
|
ENSP00000490550.1:p.Pro762Thr
|
|
ENST00000647938.1:c.4414C>A
|
ENSP00000498155.1:p.Pro1472Thr
|
|
ENST00000346085.9:c.4414C>A
|
ENSP00000344546.4:p.Pro1472Thr
|
|
ENST00000350026.9:c.4375C>A
|
ENSP00000055163.7:p.Pro1459Thr
|
|
ENST00000414678.6:c.2941C>A
|
ENSP00000412835.2:p.Pro981Thr
|
|
NM_017519.2:c.4375C>A
|
NP_059989.2:p.Pro1459Thr
|
|
NM_020732.3:c.4414C>A
|
NP_065783.3:p.Pro1472Thr
|
|
XM_005267069.3:c.4534C>A
|
XP_005267126.2:p.Pro1512Thr
|
|
XM_011535984.1:c.3613C>A
|
XP_011534286.1:p.Pro1205Thr
|
|
XM_011535985.1:c.3433C>A
|
XP_011534287.1:p.Pro1145Thr
|
|
XM_011535986.1:c.3193C>A
|
XP_011534288.1:p.Pro1065Thr
|
|
XM_011535987.1:c.2812C>A
|
XP_011534289.1:p.Pro938Thr
|
|
XM_011535988.1:c.1675C>A
|
XP_011534290.1:p.Pro559Thr
|
|
NM_001346813.1:c.4534C>A
|
NP_001333742.1:p.Pro1512Thr
|
|
NM_001363725.1:c.2284C>A
|
NP_001350654.1:p.Pro762Thr
|
|
XM_011535984.2:c.4744C>A
|
XP_011534286.2:p.Pro1582Thr
|
|
XM_011535988.3:c.1675C>A
|
XP_011534290.1:p.Pro559Thr
|
|
XM_017011103.2:c.4645C>A
|
XP_016866592.1:p.Pro1549Thr
|
|
XM_017011104.1:c.4615C>A
|
XP_016866593.1:p.Pro1539Thr
|
|
XM_017011105.2:c.4585C>A
|
XP_016866594.1:p.Pro1529Thr
|
|
XM_017011106.2:c.4456C>A
|
XP_016866595.1:p.Pro1486Thr
|
|
XM_017011107.2:c.4435C>A
|
XP_016866596.1:p.Pro1479Thr
|
|
XR_002956289.1:n.4730C>A
|
|
|
NM_001363725.2:c.2284C>A
|
NP_001350654.1:p.Pro762Thr
|
|
NM_001371656.1:c.4663C>A
|
NP_001358585.1:p.Pro1555Thr
|
|
NM_001374820.1:c.4663C>A
|
NP_001361749.1:p.Pro1555Thr
|
|
NM_001374828.1:c.4783C>A
MANE Select
|
NP_001361757.1:p.Pro1595Thr
|
|
NM_017519.3:c.4624C>A
|
NP_059989.3:p.Pro1542Thr
|
|