ENST00000262304.9:c.5443A>C
MANE Select
|
ENSP00000262304.4:p.Ser1815Arg
|
|
ENST00000262304.8:c.5443A>C
|
ENSP00000262304.4:p.Ser1815Arg
|
|
ENST00000415938.7:n.310+2616A>C
|
|
|
ENST00000423118.5:c.5443A>C
|
ENSP00000399501.1:p.Ser1815Arg
|
|
ENST00000468674.5:n.431-374A>C
|
|
|
ENST00000483024.1:c.233+2092A>C
|
|
|
ENST00000483731.5:n.790+2616A>C
|
|
|
ENST00000487932.5:c.130A>C
|
ENSP00000457132.1:p.Ser44Arg
|
|
ENST00000488185.2:c.473-1366A>C
|
|
|
ENST00000565639.6:n.773+2616A>C
|
|
|
ENST00000568591.5:c.2226+2616A>C
|
ENSP00000457162.1:n.2226+2616A>C
|
|
ENST00000569983.5:n.421+2616A>C
|
|
|
NM_000296.3:c.5443A>C
|
NP_000287.3:p.Ser1815Arg
|
|
NM_001009944.2:c.5443A>C
|
NP_001009944.2:p.Ser1815Arg
|
|
XM_005255370.2:c.2398A>C
|
XP_005255427.1:p.Ser800Arg
|
|
XM_011522525.1:c.5521A>C
|
XP_011520827.1:p.Ser1841Arg
|
|
XM_011522526.1:c.5521A>C
|
XP_011520828.1:p.Ser1841Arg
|
|
XM_011522527.1:c.5521A>C
|
XP_011520829.1:p.Ser1841Arg
|
|
XM_011522528.1:c.5497A>C
|
XP_011520830.1:p.Ser1833Arg
|
|
XM_011522529.1:c.5497A>C
|
XP_011520831.1:p.Ser1833Arg
|
|
XM_011522530.1:c.5467A>C
|
XP_011520832.1:p.Ser1823Arg
|
|
XM_011522531.1:c.5449A>C
|
XP_011520833.1:p.Ser1817Arg
|
|
XM_011522532.1:c.5395A>C
|
XP_011520834.1:p.Ser1799Arg
|
|
XM_011522533.1:c.5314A>C
|
XP_011520835.1:p.Ser1772Arg
|
|
XM_011522534.1:c.5257A>C
|
XP_011520836.1:p.Ser1753Arg
|
|
XM_011522535.1:c.3343A>C
|
XP_011520837.1:p.Ser1115Arg
|
|
XM_011522536.1:c.5521A>C
|
XP_011520838.1:p.Ser1841Arg
|
|
XM_011522537.1:c.2521A>C
|
XP_011520839.1:p.Ser841Arg
|
|
XR_932867.1:n.5536A>C
|
|
|
XR_932868.1:n.5536A>C
|
|
|
XR_932869.1:n.5536A>C
|
|
|
XR_932870.1:n.5536A>C
|
|
|
XM_005255370.3:c.2398A>C
|
XP_005255427.1:p.Ser800Arg
|
|
XM_011522528.3:c.5497A>C
|
XP_011520830.1:p.Ser1833Arg
|
|
XM_011522529.2:c.5497A>C
|
XP_011520831.1:p.Ser1833Arg
|
|
XM_011522537.2:c.2521A>C
|
XP_011520839.1:p.Ser841Arg
|
|
XM_024450298.1:c.5563A>C
|
XP_024306066.1:p.Ser1855Arg
|
|
XM_024450299.1:c.5491A>C
|
XP_024306067.1:p.Ser1831Arg
|
|
XM_024450300.1:c.5353A>C
|
XP_024306068.1:p.Ser1785Arg
|
|
XM_024450301.1:c.3439A>C
|
XP_024306069.1:p.Ser1147Arg
|
|
NM_000296.4:c.5443A>C
|
NP_000287.4:p.Ser1815Arg
|
|
NM_001009944.3:c.5443A>C
MANE Select
|
NP_001009944.3:p.Ser1815Arg
|
|