ENST00000269980.7:c.252G>C
MANE Select
|
ENSP00000269980.2:p.Arg84=
|
|
ENST00000269980.6:c.252G>C
|
ENSP00000269980.2:p.Arg84=
|
|
ENST00000457836.6:c.186G>C
|
ENSP00000416000.2:p.Arg62=
|
|
ENST00000538423.5:n.272G>C
|
|
|
ENST00000540732.3:c.354G>C
|
ENSP00000443246.1:p.Arg118=
|
|
ENST00000541315.1:c.59G>C
|
|
|
ENST00000542943.5:c.252G>C
|
ENSP00000440345.1:p.Arg84=
|
|
ENST00000595085.5:c.252G>C
|
ENSP00000471150.2:p.Arg84=
|
|
ENST00000604424.1:n.494G>C
|
|
|
NM_000709.3:c.252G>C
|
NP_000700.1:p.Arg84=
|
|
NM_001164783.1:c.252G>C
|
NP_001158255.1:p.Arg84=
|
|
NM_000709.4:c.252G>C
MANE Select
|
NP_000700.1:p.Arg84=
|
|
NM_001164783.2:c.252G>C
|
NP_001158255.1:p.Arg84=
|
|