ENST00000269980.7:c.1002G>C
MANE Select
|
ENSP00000269980.2:p.Gly334=
|
|
ENST00000269980.6:c.1002G>C
|
ENSP00000269980.2:p.Gly334=
|
|
ENST00000457836.6:c.1011G>C
|
ENSP00000416000.2:p.Gly337=
|
|
ENST00000540732.3:c.1104G>C
|
ENSP00000443246.1:p.Gly368=
|
|
ENST00000542943.5:c.915G>C
|
ENSP00000440345.1:p.Gly305=
|
|
ENST00000595085.5:c.922+307G>C
|
ENSP00000471150.2:n.922+307G>C
|
|
NM_000709.3:c.1002G>C
|
NP_000700.1:p.Gly334=
|
|
NM_001164783.1:c.999G>C
|
NP_001158255.1:p.Gly333=
|
|
NM_000709.4:c.1002G>C
MANE Select
|
NP_000700.1:p.Gly334=
|
|
NM_001164783.2:c.999G>C
|
NP_001158255.1:p.Gly333=
|
|