|
NM_001372.4:c.11176C>T
MANE Select
|
NP_001363.2:p.Arg3726Trp
|
|
ENST00000262442.9:c.11176C>T
MANE Select
|
ENSP00000262442.3:p.Arg3726Trp
|
|
NM_001372.3:c.11176C>T
|
NP_001363.2:p.Arg3726Trp
|
|
NM_004662.2:c.112C>T
|
NP_004653.2:p.Arg38Trp
|
|
ENST00000262442.8:c.11176C>T
|
ENSP00000262442.3:p.Arg3726Trp
|
|
ENST00000396001.6:n.639C>T
|
|
|
ENST00000454412.6:c.11176C>T
|
ENSP00000414874.2:p.Arg3726Trp
|
|
ENST00000581682.1:n.457C>T
|
|
|
ENST00000608377.5:c.112C>T
|
ENSP00000476951.1:p.Arg38Trp
|
|
XM_011523703.1:c.11176C>T
|
XP_011522005.1:p.Arg3726Trp
|
|
XM_011523703.2:c.11176C>T
|
XP_011522005.1:p.Arg3726Trp
|
|
XM_017024292.2:c.11059C>T
|
XP_016879781.1:p.Arg3687Trp
|
|
XM_017024293.1:c.9058C>T
|
XP_016879782.1:p.Arg3020Trp
|