ENST00000445609.7:c.859G>C
MANE Select
|
ENSP00000389879.3:p.Gly287Arg
|
|
ENST00000674677.1:c.790G>C
|
ENSP00000502265.1:p.Gly264Arg
|
|
ENST00000675067.1:c.58G>C
|
ENSP00000502817.1:p.Gly20Arg
|
|
ENST00000675356.1:n.1347G>C
|
|
|
ENST00000675752.1:n.2444G>C
|
|
|
ENST00000676028.1:c.771+1640G>C
|
ENSP00000502639.1:n.771+1640G>C
|
|
ENST00000676053.1:c.670G>C
|
ENSP00000502475.1:p.Gly224Arg
|
|
ENST00000676091.1:c.150+1640G>C
|
ENSP00000502528.1:n.150+1640G>C
|
|
ENST00000676165.1:n.2450G>C
|
|
|
ENST00000676258.1:n.1950G>C
|
|
|
ENST00000316534.8:c.1027G>C
|
ENSP00000313169.4:p.Gly343Arg
|
|
ENST00000355301.8:c.670G>C
|
ENSP00000347452.4:p.Gly224Arg
|
|
ENST00000393272.7:c.1024G>C
|
ENSP00000376953.3:p.Gly342Arg
|
|
ENST00000417665.5:c.856G>C
|
ENSP00000402176.1:p.Gly286Arg
|
|
ENST00000445609.6:c.859G>C
|
ENSP00000389879.2:p.Gly287Arg
|
|
ENST00000461707.5:n.2444G>C
|
|
|
ENST00000496524.5:n.2460G>C
|
|
|
NM_000272.3:c.1027G>C
|
NP_000263.2:p.Gly343Arg
|
|
NM_001128178.1:c.859G>C
|
NP_001121650.1:p.Gly287Arg
|
|
NM_001128179.1:c.670G>C
|
NP_001121651.1:p.Gly224Arg
|
|
NM_207181.2:c.1024G>C
|
NP_997064.2:p.Gly342Arg
|
|
XM_005263675.1:c.1024G>C
|
XP_005263732.1:p.Gly342Arg
|
|
XM_005263676.1:c.859G>C
|
XP_005263733.1:p.Gly287Arg
|
|
XM_005263677.1:c.856G>C
|
XP_005263734.1:p.Gly286Arg
|
|
XM_005263678.2:c.1027G>C
|
XP_005263735.1:p.Gly343Arg
|
|
XM_005263679.1:c.856G>C
|
XP_005263736.1:p.Gly286Arg
|
|
XM_006712551.1:c.1027G>C
|
XP_006712614.1:p.Gly343Arg
|
|
XM_006712552.2:c.1027G>C
|
XP_006712615.1:p.Gly343Arg
|
|
XM_011511244.1:c.1027G>C
|
XP_011509546.1:p.Gly343Arg
|
|
XM_017004218.1:c.859G>C
|
XP_016859707.1:p.Gly287Arg
|
|
NM_000272.4:c.1027G>C
|
NP_000263.2:p.Gly343Arg
|
|
NM_001128178.3:c.859G>C
MANE Select
|
NP_001121650.1:p.Gly287Arg
|
|
NM_001128179.2:c.670G>C
|
NP_001121651.1:p.Gly224Arg
|
|
NM_001374256.1:c.856G>C
|
NP_001361185.1:p.Gly286Arg
|
|
NM_001374257.1:c.859G>C
|
NP_001361186.1:p.Gly287Arg
|
|
NM_207181.3:c.1024G>C
|
NP_997064.2:p.Gly342Arg
|
|
NM_000272.5:c.1027G>C
|
NP_000263.2:p.Gly343Arg
|
|
NM_001128179.3:c.670G>C
|
NP_001121651.1:p.Gly224Arg
|
|
NM_207181.4:c.1024G>C
|
NP_997064.2:p.Gly342Arg
|
|