ENST00000328195.8:c.378G>T
MANE Select
|
ENSP00000333551.3:p.Val126=
|
|
ENST00000328195.7:c.378G>T
|
ENSP00000333551.3:p.Val126=
|
|
ENST00000518036.5:c.*230G>T
|
ENSP00000428005.1:n.*230G>T
|
|
ENST00000521631.1:n.61G>T
|
|
|
ENST00000523187.5:c.222G>T
|
ENSP00000427886.1:p.Val74=
|
|
ENST00000523358.5:c.378G>T
|
ENSP00000427778.1:p.Val126=
|
|
ENST00000523521.1:c.135G>T
|
ENSP00000429425.1:p.Val45=
|
|
NM_007198.3:c.378G>T
|
NP_009129.1:p.Val126=
|
|
NM_001349346.1:c.378G>T
|
NP_001336275.1:p.Val126=
|
|
NM_001349347.1:c.372G>T
|
NP_001336276.1:p.Val124=
|
|
NM_001349348.1:c.222G>T
|
NP_001336277.1:p.Val74=
|
|
NM_007198.4:c.378G>T
MANE Select
|
NP_009129.1:p.Val126=
|
|
NM_001349346.2:c.378G>T
|
NP_001336275.1:p.Val126=
|
|
NM_001349347.2:c.372G>T
|
NP_001336276.1:p.Val124=
|
|
NM_001349348.2:c.222G>T
|
NP_001336277.1:p.Val74=
|
|