ENST00000474821.2:n.3607A>T
|
|
|
ENST00000494804.2:n.3489A>T
|
|
|
ENST00000517337.2:c.1941A>T
|
ENSP00000429971.2:p.Val647=
|
|
ENST00000523444.2:c.1941A>T
|
ENSP00000428252.2:p.Val647=
|
|
ENST00000697292.1:c.2187A>T
|
ENSP00000513229.1:p.Val729=
|
|
ENST00000697293.1:c.2238A>T
|
ENSP00000513230.1:p.Val746=
|
|
ENST00000697294.1:c.*1798A>T
|
ENSP00000513231.1:n.*1798A>T
|
|
ENST00000697295.1:c.*1496A>T
|
ENSP00000513232.1:n.*1496A>T
|
|
ENST00000697296.1:c.*1855A>T
|
ENSP00000513233.1:n.*1855A>T
|
|
ENST00000697297.1:n.3972A>T
|
|
|
ENST00000697298.1:c.1941A>T
|
ENSP00000513234.1:p.Val647=
|
|
ENST00000697299.1:c.1941A>T
|
ENSP00000513235.1:p.Val647=
|
|
ENST00000697300.1:c.*1791A>T
|
ENSP00000513236.1:n.*1791A>T
|
|
ENST00000697301.1:c.*1708A>T
|
ENSP00000513237.1:n.*1708A>T
|
|
ENST00000697302.1:c.*1708A>T
|
ENSP00000513238.1:n.*1708A>T
|
|
ENST00000697303.1:c.*1791A>T
|
ENSP00000513239.1:n.*1791A>T
|
|
ENST00000697304.1:c.1875A>T
|
ENSP00000513240.1:p.Val625=
|
|
ENST00000697305.1:n.2454A>T
|
|
|
ENST00000697306.1:c.*2738A>T
|
ENSP00000513241.1:n.*2738A>T
|
|
ENST00000697307.1:c.1962A>T
|
ENSP00000513242.1:p.Val654=
|
|
ENST00000697308.1:c.2118A>T
|
ENSP00000513243.1:p.Val706=
|
|
ENST00000697309.1:c.2185-1461A>T
|
ENSP00000513244.1:n.2185-1461A>T
|
|
ENST00000697310.1:c.2187A>T
|
ENSP00000513245.1:p.Val729=
|
|
ENST00000697311.1:c.*452A>T
|
ENSP00000513246.1:n.*452A>T
|
|
ENST00000697312.1:c.*1640A>T
|
ENSP00000513247.1:n.*1640A>T
|
|
ENST00000697313.1:n.2688-1461A>T
|
|
|
ENST00000697314.1:n.3637-1461A>T
|
|
|
ENST00000697315.1:c.*91A>T
|
ENSP00000513248.1:n.*91A>T
|
|
ENST00000697316.1:n.2308A>T
|
|
|
ENST00000265433.8:c.2187A>T
MANE Select
|
ENSP00000265433.4:p.Val729=
|
|
ENST00000265433.7:c.2187A>T
|
ENSP00000265433.3:p.Val729=
|
|
ENST00000396252.6:c.*2060A>T
|
ENSP00000379551.2:n.*2060A>T
|
|
ENST00000409330.5:c.1941A>T
|
ENSP00000386924.1:p.Val647=
|
|
ENST00000474821.1:n.275A>T
|
|
|
ENST00000613033.1:c.297A>T
|
ENSP00000484487.1:p.Val99=
|
|
NM_001024688.2:c.1941A>T
|
NP_001019859.1:p.Val647=
|
|
NM_002485.4:c.2187A>T , LRG_158t1:c.2187A>T
|
NP_002476.2:p.Val729=
|
|
XM_011517044.1:c.2163A>T
|
XP_011515346.1:p.Val721=
|
|
XM_011517045.1:c.1941A>T
|
XP_011515347.1:p.Val647=
|
|
XM_017013460.1:c.1308A>T
|
XP_016868949.1:p.Val436=
|
|
XM_017013462.2:c.1308A>T
|
XP_016868951.1:p.Val436=
|
|
XM_024447163.1:c.1941A>T
|
XP_024302931.1:p.Val647=
|
|
XM_024447164.1:c.1941A>T
|
XP_024302932.1:p.Val647=
|
|
XM_024447165.1:c.1308A>T
|
XP_024302933.1:p.Val436=
|
|
NM_002485.5:c.2187A>T
MANE Select
|
NP_002476.2:p.Val729=
|
|
NM_001024688.3:c.1941A>T
|
NP_001019859.1:p.Val647=
|
|