ENST00000409709.9:c.5251C>A
MANE Select
|
ENSP00000386331.3:p.Pro1751Thr
|
|
ENST00000670577.1:c.3092C>A
|
|
|
ENST00000409619.6:c.5104C>A
|
ENSP00000386635.2:p.Pro1702Thr
|
|
ENST00000409709.7:c.5251C>A
|
ENSP00000386331.3:p.Pro1751Thr
|
|
ENST00000458169.2:c.2677C>A
|
ENSP00000417017.2:p.Pro893Thr
|
|
ENST00000458637.6:c.5137C>A
|
ENSP00000392185.2:p.Pro1713Thr
|
|
ENST00000481328.7:n.2787C>A
|
|
|
NM_000260.3:c.5251C>A
|
NP_000251.3:p.Pro1751Thr
|
|
NM_001127180.1:c.5137C>A
|
NP_001120652.1:p.Pro1713Thr
|
|
XM_005274012.2:c.5134C>A
|
XP_005274069.1:p.Pro1712Thr
|
|
XM_006718558.2:c.5242C>A
|
XP_006718621.1:p.Pro1748Thr
|
|
XM_006718559.2:c.5137C>A
|
XP_006718622.1:p.Pro1713Thr
|
|
XM_006718560.2:c.5134C>A
|
XP_006718623.1:p.Pro1712Thr
|
|
XM_006718561.2:c.5137C>A
|
XP_006718624.1:p.Pro1713Thr
|
|
XM_011545044.1:c.5251C>A
|
XP_011543346.1:p.Pro1751Thr
|
|
XM_011545045.1:c.5245C>A
|
XP_011543347.1:p.Pro1749Thr
|
|
XM_011545046.1:c.5218C>A
|
XP_011543348.1:p.Pro1740Thr
|
|
XM_011545047.1:c.5155C>A
|
XP_011543349.1:p.Pro1719Thr
|
|
XM_011545048.1:c.5026C>A
|
XP_011543350.1:p.Pro1676Thr
|
|
XM_011545049.1:c.5014C>A
|
XP_011543351.1:p.Pro1672Thr
|
|
XM_011545050.1:c.4987C>A
|
XP_011543352.1:p.Pro1663Thr
|
|
XM_011545051.1:c.5251C>A
|
XP_011543353.1:p.Pro1751Thr
|
|
XM_011545052.1:c.5251C>A
|
XP_011543354.1:p.Pro1751Thr
|
|
XR_949938.1:n.5571C>A
|
|
|
XR_949941.1:n.5571C>A
|
|
|
XR_949942.1:n.5573C>A
|
|
|
XM_011545044.2:c.5251C>A
|
XP_011543346.1:p.Pro1751Thr
|
|
XM_011545046.2:c.5341C>A
|
XP_011543348.2:p.Pro1781Thr
|
|
XM_011545050.2:c.4987C>A
|
XP_011543352.1:p.Pro1663Thr
|
|
XM_017017778.1:c.5335C>A
|
XP_016873267.1:p.Pro1779Thr
|
|
XM_017017779.1:c.5332C>A
|
XP_016873268.1:p.Pro1778Thr
|
|
XM_017017780.1:c.5341C>A
|
XP_016873269.1:p.Pro1781Thr
|
|
XM_017017781.1:c.5245C>A
|
XP_016873270.1:p.Pro1749Thr
|
|
XM_017017782.1:c.5227C>A
|
XP_016873271.1:p.Pro1743Thr
|
|
XM_017017783.1:c.5224C>A
|
XP_016873272.1:p.Pro1742Thr
|
|
XM_017017784.1:c.5224C>A
|
XP_016873273.1:p.Pro1742Thr
|
|
XM_017017785.1:c.5104C>A
|
XP_016873274.1:p.Pro1702Thr
|
|
XM_017017786.1:c.5341C>A
|
XP_016873275.1:p.Pro1781Thr
|
|
XM_017017788.1:c.5227C>A
|
XP_016873277.1:p.Pro1743Thr
|
|
XR_001747885.1:n.5356C>A
|
|
|
XR_001747886.1:n.5356C>A
|
|
|
XR_001747887.1:n.5356C>A
|
|
|
XR_001747888.1:n.5356C>A
|
|
|
NM_000260.4:c.5251C>A
MANE Select
|
NP_000251.3:p.Pro1751Thr
|
|
NM_001127180.2:c.5137C>A
|
NP_001120652.1:p.Pro1713Thr
|
|
NM_001369365.1:c.5104C>A
|
NP_001356294.1:p.Pro1702Thr
|
|