ENST00000269980.7:c.144G>C
MANE Select
|
ENSP00000269980.2:p.Leu48=
|
|
ENST00000269980.6:c.144G>C
|
ENSP00000269980.2:p.Leu48=
|
|
ENST00000457836.6:c.78G>C
|
ENSP00000416000.2:p.Leu26=
|
|
ENST00000538423.5:n.164G>C
|
|
|
ENST00000540732.3:c.246G>C
|
ENSP00000443246.1:p.Leu82=
|
|
ENST00000542943.5:c.144G>C
|
ENSP00000440345.1:p.Leu48=
|
|
ENST00000595085.5:c.144G>C
|
ENSP00000471150.2:p.Leu48=
|
|
ENST00000604424.1:n.386G>C
|
|
|
NM_000709.3:c.144G>C
|
NP_000700.1:p.Leu48=
|
|
NM_001164783.1:c.144G>C
|
NP_001158255.1:p.Leu48=
|
|
NM_000709.4:c.144G>C
MANE Select
|
NP_000700.1:p.Leu48=
|
|
NM_001164783.2:c.144G>C
|
NP_001158255.1:p.Leu48=
|
|