ENST00000394975.3:c.299G>C
MANE Select
|
ENSP00000378426.2:p.Arg100Pro
|
|
ENST00000300851.10:c.360G>C
|
ENSP00000300851.6:p.Thr120=
|
|
ENST00000319788.11:c.381G>C
|
ENSP00000326135.7:p.Thr127=
|
|
ENST00000354895.4:c.189G>C
|
ENSP00000346969.4:p.Thr63=
|
|
ENST00000394971.7:c.393G>C
|
ENSP00000378422.3:p.Thr131=
|
|
ENST00000394975.2:c.299G>C
|
ENSP00000378426.2:p.Arg100Pro
|
|
ENST00000420057.2:c.261G>C
|
|
|
ENST00000472468.1:c.-17G>C
|
ENSP00000458994.1:n.-17G>C
|
|
ENST00000498155.1:c.396G>C
|
ENSP00000417662.1:p.Thr132=
|
|
ENST00000529564.1:c.283+1985G>C
|
ENSP00000431371.1:n.283+1985G>C
|
|
ENST00000532364.1:c.173+3230G>C
|
ENSP00000460316.1:n.173+3230G>C
|
|
ENST00000533518.5:c.172G>C
|
|
|
NM_001311311.1:c.383G>C
|
NP_001298240.1:p.Arg128Pro
|
|
NM_024006.4:c.299G>C
|
NP_076869.1:p.Arg100Pro
|
|
NM_024006.5:c.299G>C
|
NP_076869.1:p.Arg100Pro
|
|
NM_206824.1:c.189G>C
|
NP_996560.1:p.Thr63=
|
|
NM_206824.2:c.189G>C
|
NP_996560.1:p.Thr63=
|
|
XM_011545944.1:c.299G>C
|
XP_011544246.1:p.Arg100Pro
|
|
XM_011545945.1:c.189G>C
|
XP_011544247.1:p.Thr63=
|
|
XR_950848.1:n.1087G>C
|
|
|
NM_024006.6:c.299G>C
MANE Select
|
NP_076869.1:p.Arg100Pro
|
|
NM_001311311.2:c.383G>C
|
NP_001298240.1:p.Arg128Pro
|
|
NM_206824.3:c.189G>C
|
NP_996560.1:p.Thr63=
|
|