ENST00000526008.6:c.*1722G=
|
ENSP00000513006.1:n.*1722G=
|
|
ENST00000696967.1:n.2342G=
|
|
|
ENST00000696968.1:n.398G=
|
|
|
ENST00000696969.1:n.2122G=
|
|
|
ENST00000458235.7:c.3165G=
MANE Select
|
ENSP00000391676.1:p.Glu1055=
|
|
ENST00000458235.5:c.3165G=
|
ENSP00000391676.1:p.Glu1055=
|
|
ENST00000527031.5:n.2279-4840G=
|
|
|
ENST00000527670.5:c.3165G=
|
ENSP00000432511.1:p.Glu1055=
|
|
ENST00000534444.1:c.3165G=
|
ENSP00000436421.1:p.Glu1055=
|
|
NM_000215.3:c.3165G= , LRG_77t1:c.3165G=
|
NP_000206.2:p.Glu1055=
|
|
XM_005259896.2:c.3294G=
|
XP_005259953.1:p.Glu1098=
|
|
XM_006722745.2:c.3165G=
|
XP_006722808.1:p.Glu1055=
|
|
XM_005259896.3:c.3294G=
|
XP_005259953.1:p.Glu1098=
|
|
NM_000215.4:c.3165G=
MANE Select
|
NP_000206.2:p.Glu1055=
|
|