|
ENST00000234071.8:c.669C>A
MANE Select
|
ENSP00000234071.4:p.Ser223Arg
|
|
|
ENST00000234071.7:c.669C>A
|
ENSP00000234071.3:p.Ser223Arg
|
|
|
ENST00000402125.2:c.121-2139C>A
|
|
|
|
ENST00000409048.1:c.771C>A
|
ENSP00000386679.1:p.Ser257Arg
|
|
|
ENST00000464089.1:n.255C>A
|
|
|
|
NM_000312.3:c.669C>A , LRG_599t1:c.669C>A
|
NP_000303.1:p.Ser223Arg
|
|
|
XM_005263715.3:c.852C>A
|
XP_005263772.1:p.Ser284Arg
|
|
|
XM_005263716.3:c.834C>A
|
XP_005263773.1:p.Ser278Arg
|
|
|
XM_005263717.3:c.732C>A
|
XP_005263774.1:p.Ser244Arg
|
|
|
XM_005263717.4:c.732C>A
|
XP_005263774.1:p.Ser244Arg
|
|
|
XM_017004505.1:c.912C>A
|
XP_016859994.1:p.Ser304Arg
|
|
|
XM_024453002.1:c.1014C>A
|
XP_024308770.1:p.Ser338Arg
|
|
|
XM_024453003.1:c.954C>A
|
XP_024308771.1:p.Ser318Arg
|
|
|
XM_024453004.1:c.852C>A
|
XP_024308772.1:p.Ser284Arg
|
|
|
XM_024453005.1:c.834C>A
|
XP_024308773.1:p.Ser278Arg
|
|
|
XM_024453006.1:c.771C>A
|
XP_024308774.1:p.Ser257Arg
|
|
|
XR_923313.2:n.4367G>T
|
|
|
|
NM_000312.4:c.669C>A
MANE Select
|
NP_000303.1:p.Ser223Arg
|
|
|
NM_001375602.1:c.852C>A
|
NP_001362531.1:p.Ser284Arg
|
|
|
NM_001375603.1:c.834C>A
|
NP_001362532.1:p.Ser278Arg
|
|
|
NM_001375604.1:c.732C>A
|
NP_001362533.1:p.Ser244Arg
|
|
|
NM_001375605.1:c.771C>A
|
NP_001362534.1:p.Ser257Arg
|
|
|
NM_001375606.1:c.837C>A
|
NP_001362535.1:p.Ser279Arg
|
|
|
NM_001375607.1:c.855C>A
|
NP_001362536.1:p.Ser285Arg
|
|
|
NM_001375608.1:c.612C>A
|
NP_001362537.1:p.Ser204Arg
|
|
|
NM_001375609.1:c.645C>A
|
NP_001362538.1:p.Ser215Arg
|
|
|
NM_001375610.1:c.663C>A
|
NP_001362539.1:p.Ser221Arg
|
|
|
NM_001375611.1:c.669C>A
|
NP_001362540.1:p.Ser223Arg
|
|
|
NM_001375613.1:c.669C>A
|
NP_001362542.1:p.Ser223Arg
|
|
