ENST00000262304.9:c.7250T>A
MANE Select
|
ENSP00000262304.4:p.Leu2417Gln
|
|
ENST00000262304.8:c.7250T>A
|
ENSP00000262304.4:p.Leu2417Gln
|
|
ENST00000415938.7:n.495T>A
|
|
|
ENST00000423118.5:c.7250T>A
|
ENSP00000399501.1:p.Leu2417Gln
|
|
ENST00000483024.1:c.418T>A
|
|
|
ENST00000483558.5:n.309T>A
|
|
|
ENST00000483731.5:n.975T>A
|
|
|
ENST00000486339.6:n.996T>A
|
|
|
ENST00000487932.5:c.1937T>A
|
ENSP00000457132.1:p.Leu646Gln
|
|
ENST00000496574.6:n.1253T>A
|
|
|
ENST00000565639.6:n.958T>A
|
|
|
ENST00000568591.5:c.2411T>A
|
ENSP00000457162.1:n.2411T>A
|
|
ENST00000569983.5:n.606T>A
|
|
|
NM_000296.3:c.7250T>A
|
NP_000287.3:p.Leu2417Gln
|
|
NM_001009944.2:c.7250T>A
|
NP_001009944.2:p.Leu2417Gln
|
|
XM_005255370.2:c.4205T>A
|
XP_005255427.1:p.Leu1402Gln
|
|
XM_011522525.1:c.7328T>A
|
XP_011520827.1:p.Leu2443Gln
|
|
XM_011522526.1:c.7328T>A
|
XP_011520828.1:p.Leu2443Gln
|
|
XM_011522527.1:c.7328T>A
|
XP_011520829.1:p.Leu2443Gln
|
|
XM_011522528.1:c.7304T>A
|
XP_011520830.1:p.Leu2435Gln
|
|
XM_011522529.1:c.7304T>A
|
XP_011520831.1:p.Leu2435Gln
|
|
XM_011522530.1:c.7274T>A
|
XP_011520832.1:p.Leu2425Gln
|
|
XM_011522531.1:c.7256T>A
|
XP_011520833.1:p.Leu2419Gln
|
|
XM_011522532.1:c.7202T>A
|
XP_011520834.1:p.Leu2401Gln
|
|
XM_011522533.1:c.7121T>A
|
XP_011520835.1:p.Leu2374Gln
|
|
XM_011522534.1:c.7064T>A
|
XP_011520836.1:p.Leu2355Gln
|
|
XM_011522535.1:c.5150T>A
|
XP_011520837.1:p.Leu1717Gln
|
|
XM_011522536.1:c.7328T>A
|
XP_011520838.1:p.Leu2443Gln
|
|
XM_011522537.1:c.4328T>A
|
XP_011520839.1:p.Leu1443Gln
|
|
XR_932867.1:n.7343T>A
|
|
|
XR_932868.1:n.7343T>A
|
|
|
XR_932869.1:n.7343T>A
|
|
|
XR_932870.1:n.7343T>A
|
|
|
XM_005255370.3:c.4205T>A
|
XP_005255427.1:p.Leu1402Gln
|
|
XM_011522528.3:c.7304T>A
|
XP_011520830.1:p.Leu2435Gln
|
|
XM_011522529.2:c.7304T>A
|
XP_011520831.1:p.Leu2435Gln
|
|
XM_011522537.2:c.4328T>A
|
XP_011520839.1:p.Leu1443Gln
|
|
XM_024450298.1:c.7370T>A
|
XP_024306066.1:p.Leu2457Gln
|
|
XM_024450299.1:c.7298T>A
|
XP_024306067.1:p.Leu2433Gln
|
|
XM_024450300.1:c.7160T>A
|
XP_024306068.1:p.Leu2387Gln
|
|
XM_024450301.1:c.5246T>A
|
XP_024306069.1:p.Leu1749Gln
|
|
NM_000296.4:c.7250T>A
|
NP_000287.4:p.Leu2417Gln
|
|
NM_001009944.3:c.7250T>A
MANE Select
|
NP_001009944.3:p.Leu2417Gln
|
|