ENST00000288774.8:c.939C>T
|
ENSP00000288774.3:p.Cys313=
|
|
ENST00000447513.7:c.879C>T
MANE Select
|
ENSP00000407922.2:p.Cys293=
|
|
ENST00000650293.1:c.833C>T
|
|
|
ENST00000288774.7:c.939C>T
|
ENSP00000288774.3:p.Cys313=
|
|
ENST00000447513.6:c.879C>T
|
ENSP00000407922.2:p.Cys293=
|
|
ENST00000507596.5:c.879C>T
|
ENSP00000424291.1:p.Cys293=
|
|
NM_002617.3:c.879C>T
|
NP_002608.1:p.Cys293=
|
|
NM_153818.1:c.939C>T
|
NP_722540.1:p.Cys313=
|
|
XM_011541573.1:c.936C>T
|
XP_011539875.1:p.Cys312=
|
|
XM_011541574.1:c.504C>T
|
XP_011539876.1:p.Cys168=
|
|
XM_011541575.1:c.504C>T
|
XP_011539877.1:p.Cys168=
|
|
XR_946666.1:n.995C>T
|
|
|
XR_946666.2:n.944C>T
|
|
|
NM_001374425.1:c.936C>T
|
NP_001361354.1:p.Cys312=
|
|
NM_001374426.1:c.504C>T
|
NP_001361355.1:p.Cys168=
|
|
NM_001374427.1:c.447C>T
|
NP_001361356.1:p.Cys149=
|
|
NM_002617.4:c.879C>T
MANE Select
|
NP_002608.1:p.Cys293=
|
|
NM_153818.2:c.939C>T
|
NP_722540.1:p.Cys313=
|
|
NR_164636.1:n.994C>T
|
|
|