ENST00000601549.2:n.519C>T
|
|
|
ENST00000648053.1:n.329C>T
|
|
|
ENST00000648319.1:c.897C>T
MANE Select
|
ENSP00000496939.1:p.His299=
|
|
ENST00000262888.7:c.897C>T
|
ENSP00000262888.3:p.His299=
|
|
ENST00000598836.1:c.76C>T
|
|
|
ENST00000599720.5:c.*167C>T
|
ENSP00000472513.1:n.*167C>T
|
|
ENST00000600408.1:c.186C>T
|
ENSP00000472510.1:p.His62=
|
|
ENST00000601549.1:n.206C>T
|
|
|
ENST00000615047.4:c.501C>T
|
ENSP00000485014.1:p.His167=
|
|
NM_002250.2:c.897C>T
|
NP_002241.1:p.His299=
|
|
XM_005258882.2:c.801C>T
|
XP_005258939.1:p.His267=
|
|
XM_005258883.2:c.708C>T
|
XP_005258940.1:p.His236=
|
|
XR_935823.1:n.2143C>T
|
|
|
XR_002958313.1:n.2289C>T
|
|
|
NM_002250.3:c.897C>T
MANE Select
|
NP_002241.1:p.His299=
|
|