ENST00000705719.1:c.180G>C
|
ENSP00000516165.1:p.Arg60=
|
|
ENST00000331134.11:c.51G>C
MANE Select
|
ENSP00000331487.5:p.Arg17=
|
|
ENST00000331134.10:c.51G>C
|
ENSP00000331487.5:p.Arg17=
|
|
ENST00000374747.9:c.51G>C
|
ENSP00000363879.5:p.Arg17=
|
|
ENST00000570300.1:n.72G>C
|
|
|
ENST00000574897.5:c.51G>C
|
ENSP00000461543.1:p.Arg17=
|
|
ENST00000625705.1:c.48G>C
|
ENSP00000486640.1:p.Arg16=
|
|
NM_017921.3:c.51G>C
|
NP_060391.2:p.Arg17=
|
|
XM_011524979.1:c.51G>C
|
XP_011523281.1:p.Arg17=
|
|
XM_011524980.1:c.51G>C
|
XP_011523282.1:p.Arg17=
|
|
XM_011524981.1:c.51G>C
|
XP_011523283.1:p.Arg17=
|
|
XM_011524982.1:c.51G>C
|
XP_011523284.1:p.Arg17=
|
|
XR_934501.1:n.269G>C
|
|
|
XR_934502.1:n.269G>C
|
|
|
XM_011524982.2:c.51G>C
|
XP_011523284.1:p.Arg17=
|
|
XR_001752557.1:n.269G>C
|
|
|
NM_017921.4:c.51G>C
MANE Select
|
NP_060391.2:p.Arg17=
|
|
NM_001369698.1:c.51G>C
|
NP_001356627.1:p.Arg17=
|
|