ENST00000426263.10:c.33C>T
MANE Select
|
ENSP00000416293.2:p.Arg11=
|
|
ENST00000674765.1:c.33C>T
|
ENSP00000501811.1:p.Arg11=
|
|
ENST00000675112.1:n.56C>T
|
|
|
ENST00000372500.4:c.19-12101C>T
|
ENSP00000361578.4:n.19-12101C>T
|
|
ENST00000415851.6:n.250C>T
|
|
|
ENST00000426263.7:c.33C>T
|
ENSP00000416293.2:p.Arg11=
|
|
ENST00000625233.2:n.241C>T
|
|
|
ENST00000628173.1:n.252C>T
|
|
|
ENST00000630287.2:c.33C>T
|
ENSP00000486694.1:p.Arg11=
|
|
ENST00000630821.1:n.250C>T
|
|
|
NM_006516.2:c.33C>T
|
NP_006507.2:p.Arg11=
|
|
NM_006516.3:c.33C>T
|
NP_006507.2:p.Arg11=
|
|
NM_006516.4:c.33C>T
MANE Select
|
NP_006507.2:p.Arg11=
|
|