ENST00000302450.11:c.936A>C
MANE Select
|
ENSP00000305204.6:p.Arg312Ser
|
|
ENST00000302450.10:c.936A>C
|
ENSP00000305204.6:p.Arg312Ser
|
|
ENST00000435431.5:c.479-301A>C
|
ENSP00000414834.1:n.479-301A>C
|
|
NM_001304361.1:c.441A>C
|
NP_001291290.1:p.Arg147Ser
|
|
NM_152515.4:c.936A>C
|
NP_689728.3:p.Arg312Ser
|
|
NR_130712.1:n.558-301A>C
|
|
|
XM_011510666.1:c.441A>C
|
XP_011508968.1:p.Arg147Ser
|
|
XM_011510666.2:c.441A>C
|
XP_011508968.1:p.Arg147Ser
|
|
NM_152515.5:c.936A>C
MANE Select
|
NP_689728.3:p.Arg312Ser
|
|
NM_001304361.2:c.441A>C
|
NP_001291290.1:p.Arg147Ser
|
|
NR_130712.2:n.490-301A>C
|
|
|