ENST00000269980.7:c.860G>C
MANE Select
|
ENSP00000269980.2:p.Arg287Pro
|
|
ENST00000269980.6:c.860G>C
|
ENSP00000269980.2:p.Arg287Pro
|
|
ENST00000457836.6:c.794G>C
|
ENSP00000416000.2:p.Arg265Pro
|
|
ENST00000535632.5:n.489G>C
|
|
|
ENST00000540732.3:c.962G>C
|
ENSP00000443246.1:p.Arg321Pro
|
|
ENST00000542943.5:c.773G>C
|
ENSP00000440345.1:p.Arg258Pro
|
|
ENST00000545787.1:n.488G>C
|
|
|
ENST00000595085.5:c.860G>C
|
ENSP00000471150.2:p.Arg287Pro
|
|
NM_000709.3:c.860G>C
|
NP_000700.1:p.Arg287Pro
|
|
NM_001164783.1:c.857G>C
|
NP_001158255.1:p.Arg286Pro
|
|
NM_000709.4:c.860G>C
MANE Select
|
NP_000700.1:p.Arg287Pro
|
|
NM_001164783.2:c.857G>C
|
NP_001158255.1:p.Arg286Pro
|
|