ENST00000601549.2:n.505G>C
|
|
|
ENST00000648053.1:n.315G>C
|
|
|
ENST00000648319.1:c.883G>C
MANE Select
|
ENSP00000496939.1:p.Glu295Gln
|
|
ENST00000262888.7:c.883G>C
|
ENSP00000262888.3:p.Glu295Gln
|
|
ENST00000598836.1:c.62G>C
|
|
|
ENST00000599720.5:c.*153G>C
|
ENSP00000472513.1:n.*153G>C
|
|
ENST00000600408.1:c.172G>C
|
ENSP00000472510.1:p.Glu58Gln
|
|
ENST00000601549.1:n.192G>C
|
|
|
ENST00000615047.4:c.487G>C
|
ENSP00000485014.1:p.Glu163Gln
|
|
NM_002250.2:c.883G>C
|
NP_002241.1:p.Glu295Gln
|
|
XM_005258882.2:c.787G>C
|
XP_005258939.1:p.Glu263Gln
|
|
XM_005258883.2:c.694G>C
|
XP_005258940.1:p.Glu232Gln
|
|
XR_935823.1:n.2129G>C
|
|
|
XR_002958313.1:n.2275G>C
|
|
|
NM_002250.3:c.883G>C
MANE Select
|
NP_002241.1:p.Glu295Gln
|
|