ENST00000332896.8:c.567G=
MANE Select
|
ENSP00000327647.3:p.Val189=
|
|
ENST00000332896.7:c.567G=
|
ENSP00000327647.3:p.Val189=
|
|
ENST00000542893.2:c.567G=
|
ENSP00000439068.2:p.Val189=
|
|
ENST00000548330.1:n.952G=
|
|
|
ENST00000548483.5:c.299-43812G=
|
ENSP00000448685.1:n.299-43812G=
|
|
ENST00000550030.1:n.367G=
|
|
|
ENST00000551065.5:c.299-9081G=
|
ENSP00000448425.1:n.299-9081G=
|
|
ENST00000609189.1:n.343G=
|
|
|
NM_003805.3:c.567G=
|
NP_003796.1:p.Val189=
|
|
XM_005269211.3:c.299-43812G=
|
XP_005269268.1:n.299-43812G=
|
|
NM_001320099.1:c.567G=
|
NP_001307028.1:p.Val189=
|
|
NM_001320100.1:c.299-43812G=
|
NP_001307029.1:n.299-43812G=
|
|
NM_003805.4:c.567G=
|
NP_003796.1:p.Val189=
|
|
NR_135147.1:n.407-9081G=
|
|
|
XM_017020144.1:c.299-9081G=
|
XP_016875633.1:n.299-9081G=
|
|
XR_001748910.1:n.430-9081G=
|
|
|
NM_003805.5:c.567G=
MANE Select
|
NP_003796.1:p.Val189=
|
|
NM_001320099.2:c.567G=
|
NP_001307028.1:p.Val189=
|
|
NM_001320100.2:c.299-43812G=
|
NP_001307029.1:n.299-43812G=
|
|
NR_135147.2:n.403-9081G=
|
|
|