ENST00000371084.8:c.408A>T
MANE Select
|
ENSP00000360125.3:p.Gly136=
|
|
ENST00000650546.1:c.408A>T
|
ENSP00000497812.1:p.Gly136=
|
|
ENST00000371083.4:c.462A>T
|
ENSP00000360124.4:p.Gly154=
|
|
ENST00000371084.7:c.408A>T
|
ENSP00000360125.3:p.Gly136=
|
|
ENST00000540265.5:c.-184A>T
|
ENSP00000443449.1:n.-184A>T
|
|
NM_001172818.1:c.462A>T
|
NP_001166289.1:p.Gly154=
|
|
NM_001172819.1:c.-184A>T
|
NP_001166290.1:n.-184A>T
|
|
NM_002633.2:c.408A>T
|
NP_002624.2:p.Gly136=
|
|
NM_002633.3:c.408A>T
MANE Select
|
NP_002624.2:p.Gly136=
|
|
NM_001172819.2:c.-184A>T
|
NP_001166290.1:n.-184A>T
|
|