ENST00000252029.8:c.399G>T
MANE Select
|
ENSP00000252029.3:p.Leu133=
|
|
ENST00000395680.6:c.399G>T
|
ENSP00000379037.1:p.Leu133=
|
|
ENST00000395681.6:c.399G>T
|
ENSP00000379038.1:p.Leu133=
|
|
ENST00000650719.1:c.399G>T
|
ENSP00000498276.1:p.Leu133=
|
|
ENST00000651095.1:n.538G>T
|
|
|
ENST00000651196.1:c.399G>T
|
ENSP00000499096.1:p.Leu133=
|
|
ENST00000651401.1:c.-1+750G>T
|
ENSP00000499115.1:n.-1+750G>T
|
|
ENST00000651906.1:n.518G>T
|
|
|
ENST00000652237.1:n.675G>T
|
|
|
ENST00000652352.1:c.147G>T
|
ENSP00000498579.1:p.Leu49=
|
|
ENST00000252029.7:c.399G>T
|
ENSP00000252029.3:p.Leu133=
|
|
ENST00000395678.7:c.399G>T
|
ENSP00000379036.3:p.Leu133=
|
|
ENST00000395680.5:c.399G>T
|
ENSP00000379037.1:p.Leu133=
|
|
ENST00000395681.5:c.399G>T
|
ENSP00000379038.1:p.Leu133=
|
|
ENST00000425169.1:c.399G>T
|
ENSP00000395875.1:p.Leu133=
|
|
ENST00000476284.1:n.524G>T
|
|
|
ENST00000487162.1:n.687G>T
|
|
|
ENST00000487577.5:n.686G>T
|
|
|
NM_001113755.2:c.399G>T
|
NP_001107227.1:p.Leu133=
|
|
NM_001113756.2:c.399G>T
|
NP_001107228.1:p.Leu133=
|
|
NM_001257988.1:c.399G>T , LRG_727t1:c.399G>T
|
NP_001244917.1:p.Leu133=
|
|
NM_001257989.1:c.399G>T , LRG_727t2:c.399G>T
|
NP_001244918.1:p.Leu133=
|
|
NM_001953.4:c.399G>T
|
NP_001944.1:p.Leu133=
|
|
NM_001113755.3:c.399G>T
|
NP_001107227.1:p.Leu133=
|
|
NM_001113756.3:c.399G>T
|
NP_001107228.1:p.Leu133=
|
|
NM_001953.5:c.399G>T
MANE Select
|
NP_001944.1:p.Leu133=
|
|