ENST00000269980.7:c.444G>T
MANE Select
|
ENSP00000269980.2:p.Leu148=
|
|
ENST00000269980.6:c.444G>T
|
ENSP00000269980.2:p.Leu148=
|
|
ENST00000457836.6:c.378G>T
|
ENSP00000416000.2:p.Leu126=
|
|
ENST00000538423.5:n.570G>T
|
|
|
ENST00000540732.3:c.546G>T
|
ENSP00000443246.1:p.Leu182=
|
|
ENST00000541315.1:c.251G>T
|
|
|
ENST00000542943.5:c.357G>T
|
ENSP00000440345.1:p.Leu119=
|
|
ENST00000595085.5:c.444G>T
|
ENSP00000471150.2:p.Leu148=
|
|
NM_000709.3:c.444G>T
|
NP_000700.1:p.Leu148=
|
|
NM_001164783.1:c.444G>T
|
NP_001158255.1:p.Leu148=
|
|
NM_000709.4:c.444G>T
MANE Select
|
NP_000700.1:p.Leu148=
|
|
NM_001164783.2:c.444G>T
|
NP_001158255.1:p.Leu148=
|
|