ENST00000262304.9:c.7244T>A
MANE Select
|
ENSP00000262304.4:p.Leu2415Gln
|
|
ENST00000262304.8:c.7244T>A
|
ENSP00000262304.4:p.Leu2415Gln
|
|
ENST00000415938.7:n.489T>A
|
|
|
ENST00000423118.5:c.7244T>A
|
ENSP00000399501.1:p.Leu2415Gln
|
|
ENST00000483024.1:c.412T>A
|
|
|
ENST00000483558.5:n.303T>A
|
|
|
ENST00000483731.5:n.969T>A
|
|
|
ENST00000486339.6:n.990T>A
|
|
|
ENST00000487932.5:c.1931T>A
|
ENSP00000457132.1:p.Leu644Gln
|
|
ENST00000496574.6:n.1247T>A
|
|
|
ENST00000565639.6:n.952T>A
|
|
|
ENST00000568591.5:c.2405T>A
|
ENSP00000457162.1:n.2405T>A
|
|
ENST00000569983.5:n.600T>A
|
|
|
NM_000296.3:c.7244T>A
|
NP_000287.3:p.Leu2415Gln
|
|
NM_001009944.2:c.7244T>A
|
NP_001009944.2:p.Leu2415Gln
|
|
XM_005255370.2:c.4199T>A
|
XP_005255427.1:p.Leu1400Gln
|
|
XM_011522525.1:c.7322T>A
|
XP_011520827.1:p.Leu2441Gln
|
|
XM_011522526.1:c.7322T>A
|
XP_011520828.1:p.Leu2441Gln
|
|
XM_011522527.1:c.7322T>A
|
XP_011520829.1:p.Leu2441Gln
|
|
XM_011522528.1:c.7298T>A
|
XP_011520830.1:p.Leu2433Gln
|
|
XM_011522529.1:c.7298T>A
|
XP_011520831.1:p.Leu2433Gln
|
|
XM_011522530.1:c.7268T>A
|
XP_011520832.1:p.Leu2423Gln
|
|
XM_011522531.1:c.7250T>A
|
XP_011520833.1:p.Leu2417Gln
|
|
XM_011522532.1:c.7196T>A
|
XP_011520834.1:p.Leu2399Gln
|
|
XM_011522533.1:c.7115T>A
|
XP_011520835.1:p.Leu2372Gln
|
|
XM_011522534.1:c.7058T>A
|
XP_011520836.1:p.Leu2353Gln
|
|
XM_011522535.1:c.5144T>A
|
XP_011520837.1:p.Leu1715Gln
|
|
XM_011522536.1:c.7322T>A
|
XP_011520838.1:p.Leu2441Gln
|
|
XM_011522537.1:c.4322T>A
|
XP_011520839.1:p.Leu1441Gln
|
|
XR_932867.1:n.7337T>A
|
|
|
XR_932868.1:n.7337T>A
|
|
|
XR_932869.1:n.7337T>A
|
|
|
XR_932870.1:n.7337T>A
|
|
|
XM_005255370.3:c.4199T>A
|
XP_005255427.1:p.Leu1400Gln
|
|
XM_011522528.3:c.7298T>A
|
XP_011520830.1:p.Leu2433Gln
|
|
XM_011522529.2:c.7298T>A
|
XP_011520831.1:p.Leu2433Gln
|
|
XM_011522537.2:c.4322T>A
|
XP_011520839.1:p.Leu1441Gln
|
|
XM_024450298.1:c.7364T>A
|
XP_024306066.1:p.Leu2455Gln
|
|
XM_024450299.1:c.7292T>A
|
XP_024306067.1:p.Leu2431Gln
|
|
XM_024450300.1:c.7154T>A
|
XP_024306068.1:p.Leu2385Gln
|
|
XM_024450301.1:c.5240T>A
|
XP_024306069.1:p.Leu1747Gln
|
|
NM_000296.4:c.7244T>A
|
NP_000287.4:p.Leu2415Gln
|
|
NM_001009944.3:c.7244T>A
MANE Select
|
NP_001009944.3:p.Leu2415Gln
|
|