ENST00000328195.8:c.222A>T
MANE Select
|
ENSP00000333551.3:p.Leu74=
|
|
ENST00000328195.7:c.222A>T
|
ENSP00000333551.3:p.Leu74=
|
|
ENST00000518036.5:c.*74A>T
|
ENSP00000428005.1:n.*74A>T
|
|
ENST00000520073.5:n.287A>T
|
|
|
ENST00000523187.5:c.66A>T
|
ENSP00000427886.1:p.Leu22=
|
|
ENST00000523358.5:c.222A>T
|
ENSP00000427778.1:p.Leu74=
|
|
ENST00000523994.1:n.227A>T
|
|
|
NM_007198.3:c.222A>T
|
NP_009129.1:p.Leu74=
|
|
NM_001349346.1:c.222A>T
|
NP_001336275.1:p.Leu74=
|
|
NM_001349347.1:c.216A>T
|
NP_001336276.1:p.Leu72=
|
|
NM_001349348.1:c.66A>T
|
NP_001336277.1:p.Leu22=
|
|
NM_001349349.1:c.327A>T
|
NP_001336278.1:p.Leu109=
|
|
NM_007198.4:c.222A>T
MANE Select
|
NP_009129.1:p.Leu74=
|
|
NM_001349346.2:c.222A>T
|
NP_001336275.1:p.Leu74=
|
|
NM_001349347.2:c.216A>T
|
NP_001336276.1:p.Leu72=
|
|
NM_001349348.2:c.66A>T
|
NP_001336277.1:p.Leu22=
|
|