ENST00000262494.13:c.534C>A
|
ENSP00000262494.7:p.Thr178=
|
|
ENST00000262493.12:c.534C>A
MANE Select
|
ENSP00000262493.6:p.Thr178=
|
|
ENST00000262494.12:c.534C>A
|
ENSP00000262494.7:p.Thr178=
|
|
ENST00000562316.6:c.201C>A
|
ENSP00000457238.2:p.Thr67=
|
|
ENST00000638185.1:n.749C>A
|
|
|
ENST00000638210.1:n.834C>A
|
|
|
ENST00000638705.1:c.534C>A
|
ENSP00000491223.1:p.Thr178=
|
|
ENST00000638836.1:n.444C>A
|
|
|
ENST00000639055.1:n.1255C>A
|
|
|
ENST00000639251.1:n.435C>A
|
|
|
ENST00000639268.1:c.229-1933C>A
|
|
|
ENST00000639341.1:c.59C>A
|
|
|
ENST00000639770.1:c.572C>A
|
ENSP00000491999.1:n.572C>A
|
|
ENST00000640390.1:n.464C>A
|
|
|
ENST00000640893.1:c.373C>A
|
ENSP00000492677.1:p.Gln125Lys
|
|
ENST00000262493.10:c.534C>A
|
ENSP00000262493.6:p.Thr178=
|
|
ENST00000262494.11:c.534C>A
|
ENSP00000262494.7:p.Thr178=
|
|
ENST00000562316.5:c.273C>A
|
ENSP00000457238.1:p.Thr91=
|
|
NM_020988.2:c.534C>A
|
NP_066268.1:p.Thr178=
|
|
NM_138736.2:c.534C>A
|
NP_620073.2:p.Thr178=
|
|
XM_011523003.1:c.408C>A
|
XP_011521305.1:p.Thr136=
|
|
XM_011523003.3:c.408C>A
|
XP_011521305.1:p.Thr136=
|
|
NM_020988.3:c.534C>A
MANE Select
|
NP_066268.1:p.Thr178=
|
|
NM_138736.3:c.534C>A
|
NP_620073.2:p.Thr178=
|
|