ENST00000461050.6:c.*95A>T
|
ENSP00000476319.1:n.*95A>T
|
|
ENST00000539040.6:c.258A>T
|
ENSP00000441950.1:p.Arg86=
|
|
ENST00000704061.1:c.*37A>T
|
ENSP00000515664.1:n.*37A>T
|
|
ENST00000368323.8:c.366A>T
MANE Select
|
ENSP00000357306.3:p.Arg122=
|
|
ENST00000651833.1:c.366A>T
|
ENSP00000498732.1:p.Arg122=
|
|
ENST00000651853.1:c.369A>T
|
ENSP00000498685.1:p.Arg123=
|
|
ENST00000368322.7:c.417A>T
|
ENSP00000357305.3:p.Arg139=
|
|
ENST00000368323.7:c.366A>T
|
ENSP00000357306.3:p.Arg122=
|
|
ENST00000461050.5:c.*95A>T
|
ENSP00000476319.1:n.*95A>T
|
|
ENST00000539040.5:c.258A>T
|
ENSP00000441950.1:p.Arg86=
|
|
ENST00000609492.1:c.366A>T
|
ENSP00000476612.1:p.Arg122=
|
|
NM_001256820.1:c.258A>T
|
NP_001243749.1:p.Arg86=
|
|
NM_001256821.1:c.417A>T
|
NP_001243750.1:p.Arg139=
|
|
NM_006912.5:c.366A>T
|
NP_008843.1:p.Arg122=
|
|
NM_001256820.2:c.258A>T
|
NP_001243749.1:p.Arg86=
|
|
NM_001256821.2:c.417A>T
|
NP_001243750.1:p.Arg139=
|
|
NM_006912.6:c.366A>T
MANE Select
|
NP_008843.1:p.Arg122=
|
|