|
NM_006767.4:c.1055A>C
MANE Select
|
NP_006758.2:p.Tyr352Ser
|
|
ENST00000646124.2:c.1055A>C
MANE Select
|
ENSP00000496779.1:p.Tyr352Ser
|
|
NM_006767.3:c.1055A>C
|
NP_006758.2:p.Tyr352Ser
|
|
ENST00000215739.12:c.1055A>C
|
ENSP00000215739.8:p.Tyr352Ser
|
|
ENST00000461510.1:n.156A>C
|
|
|
ENST00000479606.5:n.1201A>C
|
|
|
ENST00000492480.1:n.111A>C
|
|
|
ENST00000495142.6:n.400A>C
|
|
|
ENST00000497716.5:n.882A>C
|
|
|
ENST00000642151.1:c.886A>C
|
|
|
ENST00000643578.1:n.1077A>C
|
|
|
ENST00000646506.1:n.634A>C
|
|
|
ENST00000700578.1:c.1055A>C
|
ENSP00000515073.1:p.Tyr352Ser
|