ENST00000409709.9:c.6118C>G
MANE Select
|
ENSP00000386331.3:p.Leu2040Val
|
|
ENST00000670577.1:c.3919C>G
|
|
|
ENST00000409619.6:c.5971C>G
|
ENSP00000386635.2:p.Leu1991Val
|
|
ENST00000409709.7:c.6118C>G
|
ENSP00000386331.3:p.Leu2040Val
|
|
ENST00000458169.2:c.3544C>G
|
ENSP00000417017.2:p.Leu1182Val
|
|
ENST00000458637.6:c.6004C>G
|
ENSP00000392185.2:p.Leu2002Val
|
|
ENST00000481328.7:n.3654C>G
|
|
|
ENST00000526863.2:n.25+307C>G
|
|
|
ENST00000605744.1:n.1585C>G
|
|
|
NM_000260.3:c.6118C>G
|
NP_000251.3:p.Leu2040Val
|
|
NM_001127180.1:c.6004C>G
|
NP_001120652.1:p.Leu2002Val
|
|
XM_005274012.2:c.6001C>G
|
XP_005274069.1:p.Leu2001Val
|
|
XM_006718558.2:c.6109C>G
|
XP_006718621.1:p.Leu2037Val
|
|
XM_006718559.2:c.6004C>G
|
XP_006718622.1:p.Leu2002Val
|
|
XM_006718560.2:c.6001C>G
|
XP_006718623.1:p.Leu2001Val
|
|
XM_006718561.2:c.6004C>G
|
XP_006718624.1:p.Leu2002Val
|
|
XM_011545044.1:c.6118C>G
|
XP_011543346.1:p.Leu2040Val
|
|
XM_011545045.1:c.6112C>G
|
XP_011543347.1:p.Leu2038Val
|
|
XM_011545046.1:c.6085C>G
|
XP_011543348.1:p.Leu2029Val
|
|
XM_011545047.1:c.6022C>G
|
XP_011543349.1:p.Leu2008Val
|
|
XM_011545048.1:c.5893C>G
|
XP_011543350.1:p.Leu1965Val
|
|
XM_011545049.1:c.5881C>G
|
XP_011543351.1:p.Leu1961Val
|
|
XM_011545050.1:c.5854C>G
|
XP_011543352.1:p.Leu1952Val
|
|
XM_011545051.1:c.6118C>G
|
XP_011543353.1:p.Leu2040Val
|
|
XR_949938.1:n.6438C>G
|
|
|
XR_949941.1:n.6412C>G
|
|
|
XM_011545044.2:c.6118C>G
|
XP_011543346.1:p.Leu2040Val
|
|
XM_011545046.2:c.6208C>G
|
XP_011543348.2:p.Leu2070Val
|
|
XM_011545050.2:c.5854C>G
|
XP_011543352.1:p.Leu1952Val
|
|
XM_017017778.1:c.6202C>G
|
XP_016873267.1:p.Leu2068Val
|
|
XM_017017779.1:c.6199C>G
|
XP_016873268.1:p.Leu2067Val
|
|
XM_017017780.1:c.6208C>G
|
XP_016873269.1:p.Leu2070Val
|
|
XM_017017781.1:c.6112C>G
|
XP_016873270.1:p.Leu2038Val
|
|
XM_017017782.1:c.6094C>G
|
XP_016873271.1:p.Leu2032Val
|
|
XM_017017783.1:c.6091C>G
|
XP_016873272.1:p.Leu2031Val
|
|
XM_017017784.1:c.6091C>G
|
XP_016873273.1:p.Leu2031Val
|
|
XM_017017785.1:c.5971C>G
|
XP_016873274.1:p.Leu1991Val
|
|
XM_017017786.1:c.6208C>G
|
XP_016873275.1:p.Leu2070Val
|
|
XM_017017788.1:c.6094C>G
|
XP_016873277.1:p.Leu2032Val
|
|
XR_001747885.1:n.6197C>G
|
|
|
XR_001747886.1:n.6138C>G
|
|
|
XR_001747887.1:n.6183C>G
|
|
|
NM_000260.4:c.6118C>G
MANE Select
|
NP_000251.3:p.Leu2040Val
|
|
NM_001127180.2:c.6004C>G
|
NP_001120652.1:p.Leu2002Val
|
|
NM_001369365.1:c.5971C>G
|
NP_001356294.1:p.Leu1991Val
|
|