ENST00000688602.1:c.930C>T
|
|
|
ENST00000689936.1:c.912C>T
|
|
|
ENST00000359596.8:c.12520C>T
MANE Select
|
ENSP00000352608.2:p.Arg4174Cys
|
|
ENST00000355481.8:c.12505C>T
|
ENSP00000347667.3:p.Arg4169Cys
|
|
ENST00000359596.7:c.12520C>T
|
ENSP00000352608.2:p.Arg4174Cys
|
|
ENST00000360985.7:c.12502C>T
|
ENSP00000354254.4:p.Arg4168Cys
|
|
ENST00000594335.5:c.5889C>T
|
|
|
NM_000540.2:c.12520C>T , LRG_766t1:c.12520C>T
|
NP_000531.2:p.Arg4174Cys
|
|
NM_001042723.1:c.12505C>T
|
NP_001036188.1:p.Arg4169Cys
|
|
XM_006723317.1:c.12502C>T
|
XP_006723380.1:p.Arg4168Cys
|
|
XM_006723319.1:c.12487C>T
|
XP_006723382.1:p.Arg4163Cys
|
|
XM_011527204.1:c.12517C>T
|
XP_011525506.1:p.Arg4173Cys
|
|
XM_011527205.1:c.12520C>T
|
XP_011525507.1:p.Arg4174Cys
|
|
XM_006723317.2:c.12502C>T
|
XP_006723380.1:p.Arg4168Cys
|
|
XM_006723319.2:c.12487C>T
|
XP_006723382.1:p.Arg4163Cys
|
|
XM_011527205.2:c.12520C>T
|
XP_011525507.1:p.Arg4174Cys
|
|
NM_000540.3:c.12520C>T
MANE Select
|
NP_000531.2:p.Arg4174Cys
|
|
NM_001042723.2:c.12505C>T
|
NP_001036188.1:p.Arg4169Cys
|
|