ENST00000350026.11:c.4870C>A
|
ENSP00000055163.8:p.Pro1624Thr
|
|
ENST00000414678.8:c.4939C>A
|
ENSP00000412835.3:p.Pro1647Thr
|
|
ENST00000637015.2:c.5158C>A
|
ENSP00000489729.2:p.Pro1720Thr
|
|
ENST00000346085.10:c.4909C>A
|
ENSP00000344546.5:p.Pro1637Thr
|
|
ENST00000350026.10:c.4621C>A
|
ENSP00000055163.7:p.Pro1541Thr
|
|
ENST00000414678.7:c.3187C>A
|
ENSP00000412835.2:p.Pro1063Thr
|
|
ENST00000635849.1:c.2350C>A
|
ENSP00000490948.1:p.Pro784Thr
|
|
ENST00000635957.1:c.1981C>A
|
ENSP00000490385.1:p.Pro661Thr
|
|
ENST00000636227.1:n.3492C>A
|
|
|
ENST00000636254.1:n.949C>A
|
|
|
ENST00000636930.2:c.5029C>A
MANE Select
|
ENSP00000490491.2:p.Pro1677Thr
|
|
ENST00000636940.1:n.3026C>A
|
|
|
ENST00000637015.1:c.2397C>A
|
|
|
ENST00000637568.1:c.2311C>A
|
|
|
ENST00000637741.1:n.1695C>A
|
|
|
ENST00000637810.1:c.2371C>A
|
ENSP00000489636.1:p.Pro791Thr
|
|
ENST00000637904.1:c.2530C>A
|
ENSP00000490550.1:p.Pro844Thr
|
|
ENST00000647938.1:c.4660C>A
|
ENSP00000498155.1:p.Pro1554Thr
|
|
ENST00000346085.9:c.4660C>A
|
ENSP00000344546.4:p.Pro1554Thr
|
|
ENST00000350026.9:c.4621C>A
|
ENSP00000055163.7:p.Pro1541Thr
|
|
ENST00000414678.6:c.3187C>A
|
ENSP00000412835.2:p.Pro1063Thr
|
|
NM_017519.2:c.4621C>A
|
NP_059989.2:p.Pro1541Thr
|
|
NM_020732.3:c.4660C>A
|
NP_065783.3:p.Pro1554Thr
|
|
XM_005267069.3:c.4780C>A
|
XP_005267126.2:p.Pro1594Thr
|
|
XM_011535984.1:c.3859C>A
|
XP_011534286.1:p.Pro1287Thr
|
|
XM_011535985.1:c.3679C>A
|
XP_011534287.1:p.Pro1227Thr
|
|
XM_011535986.1:c.3439C>A
|
XP_011534288.1:p.Pro1147Thr
|
|
XM_011535987.1:c.3058C>A
|
XP_011534289.1:p.Pro1020Thr
|
|
XM_011535988.1:c.1921C>A
|
XP_011534290.1:p.Pro641Thr
|
|
NM_001346813.1:c.4780C>A
|
NP_001333742.1:p.Pro1594Thr
|
|
NM_001363725.1:c.2530C>A
|
NP_001350654.1:p.Pro844Thr
|
|
XM_011535984.2:c.4990C>A
|
XP_011534286.2:p.Pro1664Thr
|
|
XM_011535988.3:c.1921C>A
|
XP_011534290.1:p.Pro641Thr
|
|
XM_017011103.2:c.4891C>A
|
XP_016866592.1:p.Pro1631Thr
|
|
XM_017011104.1:c.4861C>A
|
XP_016866593.1:p.Pro1621Thr
|
|
XM_017011105.2:c.4831C>A
|
XP_016866594.1:p.Pro1611Thr
|
|
XM_017011106.2:c.4702C>A
|
XP_016866595.1:p.Pro1568Thr
|
|
XM_017011107.2:c.4681C>A
|
XP_016866596.1:p.Pro1561Thr
|
|
XR_002956289.1:n.4976C>A
|
|
|
NM_001363725.2:c.2530C>A
|
NP_001350654.1:p.Pro844Thr
|
|
NM_001371656.1:c.4909C>A
|
NP_001358585.1:p.Pro1637Thr
|
|
NM_001374820.1:c.4909C>A
|
NP_001361749.1:p.Pro1637Thr
|
|
NM_001374828.1:c.5029C>A
MANE Select
|
NP_001361757.1:p.Pro1677Thr
|
|
NM_017519.3:c.4870C>A
|
NP_059989.3:p.Pro1624Thr
|
|