ENST00000503581.6:c.6906T>C
MANE Select
|
ENSP00000424243.1:p.Val2302=
|
|
ENST00000370616.6:c.6906T>C
|
ENSP00000359650.2:p.Val2302=
|
|
ENST00000370618.7:c.6906T>C
|
ENSP00000359652.4:p.Val2302=
|
|
ENST00000370621.7:c.6906T>C
|
ENSP00000359655.3:p.Val2302=
|
|
ENST00000398580.3:c.220T>C
|
|
|
ENST00000503581.5:c.6906T>C
|
ENSP00000424243.1:p.Val2302=
|
|
NM_001142800.1:c.6906T>C
|
NP_001136272.1:p.Val2302=
|
|
NM_001292009.1:c.6906T>C
|
NP_001278938.1:p.Val2302=
|
|
XR_001744188.1:n.606+16248A>G
|
|
|
XR_001744189.1:n.129+16248A>G
|
|
|
XR_001744190.1:n.197+16248A>G
|
|
|
XR_001744191.1:n.607-1122A>G
|
|
|
NM_001142800.2:c.6906T>C
MANE Select
|
NP_001136272.1:p.Val2302=
|
|
NM_001292009.2:c.6906T>C
|
NP_001278938.1:p.Val2302=
|
|