ENST00000406757.3:c.23C>T
|
|
|
ENST00000684880.1:c.*422C>T
|
ENSP00000510280.1:n.*422C>T
|
|
ENST00000689310.1:c.786C>T
|
ENSP00000510438.1:p.Cys262=
|
|
ENST00000692084.1:c.28C>T
|
|
|
ENST00000370818.8:c.834C>T
MANE Select
|
ENSP00000359854.3:p.Cys278=
|
|
ENST00000394299.7:c.834C>T
|
ENSP00000377836.2:p.Cys278=
|
|
ENST00000666673.1:n.28C>T
|
|
|
ENST00000370818.7:c.834C>T
|
ENSP00000359854.3:p.Cys278=
|
|
ENST00000394299.6:c.834C>T
|
ENSP00000377836.2:p.Cys278=
|
|
ENST00000406757.2:c.23C>T
|
|
|
ENST00000631057.2:c.672C>T
|
ENSP00000486325.1:p.Cys224=
|
|
NM_001164617.1:c.834C>T
|
NP_001158089.1:p.Cys278=
|
|
NM_001164618.1:c.786C>T
|
NP_001158090.1:p.Cys262=
|
|
NM_001164619.1:c.672C>T
|
NP_001158091.1:p.Cys224=
|
|
NM_004484.3:c.834C>T , LRG_505t1:c.834C>T
|
NP_004475.1:p.Cys278=
|
|
XM_017029413.2:c.834C>T
|
XP_016884902.1:p.Cys278=
|
|
NM_001164617.2:c.834C>T
|
NP_001158089.1:p.Cys278=
|
|
NM_001164618.2:c.786C>T
|
NP_001158090.1:p.Cys262=
|
|
NM_001164619.2:c.672C>T
|
NP_001158091.1:p.Cys224=
|
|
NM_004484.4:c.834C>T
MANE Select
|
NP_004475.1:p.Cys278=
|
|