ENST00000409709.9:c.5246G>A
MANE Select
|
ENSP00000386331.3:p.Arg1749Gln
|
|
ENST00000670577.1:c.3087G>A
|
|
|
ENST00000409619.6:c.5099G>A
|
ENSP00000386635.2:p.Arg1700Gln
|
|
ENST00000409709.7:c.5246G>A
|
ENSP00000386331.3:p.Arg1749Gln
|
|
ENST00000458169.2:c.2672G>A
|
ENSP00000417017.2:p.Arg891Gln
|
|
ENST00000458637.6:c.5132G>A
|
ENSP00000392185.2:p.Arg1711Gln
|
|
ENST00000481328.7:n.2782G>A
|
|
|
NM_000260.3:c.5246G>A
|
NP_000251.3:p.Arg1749Gln
|
|
NM_001127180.1:c.5132G>A
|
NP_001120652.1:p.Arg1711Gln
|
|
XM_005274012.2:c.5129G>A
|
XP_005274069.1:p.Arg1710Gln
|
|
XM_006718558.2:c.5237G>A
|
XP_006718621.1:p.Arg1746Gln
|
|
XM_006718559.2:c.5132G>A
|
XP_006718622.1:p.Arg1711Gln
|
|
XM_006718560.2:c.5129G>A
|
XP_006718623.1:p.Arg1710Gln
|
|
XM_006718561.2:c.5132G>A
|
XP_006718624.1:p.Arg1711Gln
|
|
XM_011545044.1:c.5246G>A
|
XP_011543346.1:p.Arg1749Gln
|
|
XM_011545045.1:c.5240G>A
|
XP_011543347.1:p.Arg1747Gln
|
|
XM_011545046.1:c.5213G>A
|
XP_011543348.1:p.Arg1738Gln
|
|
XM_011545047.1:c.5150G>A
|
XP_011543349.1:p.Arg1717Gln
|
|
XM_011545048.1:c.5021G>A
|
XP_011543350.1:p.Arg1674Gln
|
|
XM_011545049.1:c.5009G>A
|
XP_011543351.1:p.Arg1670Gln
|
|
XM_011545050.1:c.4982G>A
|
XP_011543352.1:p.Arg1661Gln
|
|
XM_011545051.1:c.5246G>A
|
XP_011543353.1:p.Arg1749Gln
|
|
XM_011545052.1:c.5246G>A
|
XP_011543354.1:p.Arg1749Gln
|
|
XR_949938.1:n.5566G>A
|
|
|
XR_949941.1:n.5566G>A
|
|
|
XR_949942.1:n.5568G>A
|
|
|
XM_011545044.2:c.5246G>A
|
XP_011543346.1:p.Arg1749Gln
|
|
XM_011545046.2:c.5336G>A
|
XP_011543348.2:p.Arg1779Gln
|
|
XM_011545050.2:c.4982G>A
|
XP_011543352.1:p.Arg1661Gln
|
|
XM_017017778.1:c.5330G>A
|
XP_016873267.1:p.Arg1777Gln
|
|
XM_017017779.1:c.5327G>A
|
XP_016873268.1:p.Arg1776Gln
|
|
XM_017017780.1:c.5336G>A
|
XP_016873269.1:p.Arg1779Gln
|
|
XM_017017781.1:c.5240G>A
|
XP_016873270.1:p.Arg1747Gln
|
|
XM_017017782.1:c.5222G>A
|
XP_016873271.1:p.Arg1741Gln
|
|
XM_017017783.1:c.5219G>A
|
XP_016873272.1:p.Arg1740Gln
|
|
XM_017017784.1:c.5219G>A
|
XP_016873273.1:p.Arg1740Gln
|
|
XM_017017785.1:c.5099G>A
|
XP_016873274.1:p.Arg1700Gln
|
|
XM_017017786.1:c.5336G>A
|
XP_016873275.1:p.Arg1779Gln
|
|
XM_017017788.1:c.5222G>A
|
XP_016873277.1:p.Arg1741Gln
|
|
XR_001747885.1:n.5351G>A
|
|
|
XR_001747886.1:n.5351G>A
|
|
|
XR_001747887.1:n.5351G>A
|
|
|
XR_001747888.1:n.5351G>A
|
|
|
NM_000260.4:c.5246G>A
MANE Select
|
NP_000251.3:p.Arg1749Gln
|
|
NM_001127180.2:c.5132G>A
|
NP_001120652.1:p.Arg1711Gln
|
|
NM_001369365.1:c.5099G>A
|
NP_001356294.1:p.Arg1700Gln
|
|