ENST00000289473.11:c.1102C>T
MANE Select
|
ENSP00000289473.4:p.Arg368Trp
|
|
ENST00000289473.10:c.1102C>T
|
ENSP00000289473.4:p.Arg368Trp
|
|
ENST00000289473.8:c.1102C>T
|
ENSP00000289473.4:p.Arg368Trp
|
|
ENST00000398421.6:n.2129C>T
|
|
|
ENST00000455062.2:n.1211C>T
|
|
|
NM_000265.5:c.1102C>T
|
NP_000256.4:p.Arg368Trp
|
|
XM_005250543.3:c.*23C>T
|
XP_005250600.2:n.*23C>T
|
|
XM_011516498.1:c.1101C>T
|
XP_011514800.1:p.Arg367=
|
|
XM_011516501.1:c.709C>T
|
XP_011514803.1:p.Arg237Trp
|
|
NM_000265.6:c.1102C>T
|
NP_000256.4:p.Arg368Trp
|
|
NM_000265.7:c.1102C>T
MANE Select
|
NP_000256.4:p.Arg368Trp
|
|