ENST00000593677.2:c.869C>T
|
|
|
ENST00000688602.1:c.2266C>T
|
|
|
ENST00000689936.1:c.2238C>T
|
|
|
ENST00000359596.8:c.13933C>T
MANE Select
|
ENSP00000352608.2:p.Arg4645Trp
|
|
ENST00000355481.8:c.13918C>T
|
ENSP00000347667.3:p.Arg4640Trp
|
|
ENST00000359596.7:c.13933C>T
|
ENSP00000352608.2:p.Arg4645Trp
|
|
ENST00000360985.7:c.13915C>T
|
ENSP00000354254.4:p.Arg4639Trp
|
|
ENST00000593677.1:c.393C>T
|
|
|
NM_000540.2:c.13933C>T , LRG_766t1:c.13933C>T
|
NP_000531.2:p.Arg4645Trp
|
|
NM_001042723.1:c.13918C>T
|
NP_001036188.1:p.Arg4640Trp
|
|
XM_006723317.1:c.13915C>T
|
XP_006723380.1:p.Arg4639Trp
|
|
XM_006723319.1:c.13900C>T
|
XP_006723382.1:p.Arg4634Trp
|
|
XM_011527204.1:c.13930C>T
|
XP_011525506.1:p.Arg4644Trp
|
|
XM_011527205.1:c.13846C>T
|
XP_011525507.1:p.Arg4616Trp
|
|
XM_006723317.2:c.13915C>T
|
XP_006723380.1:p.Arg4639Trp
|
|
XM_006723319.2:c.13900C>T
|
XP_006723382.1:p.Arg4634Trp
|
|
XM_011527205.2:c.13846C>T
|
XP_011525507.1:p.Arg4616Trp
|
|
NM_000540.3:c.13933C>T
MANE Select
|
NP_000531.2:p.Arg4645Trp
|
|
NM_001042723.2:c.13918C>T
|
NP_001036188.1:p.Arg4640Trp
|
|