ENST00000684880.1:c.*349G=
|
ENSP00000510280.1:n.*349G=
|
|
ENST00000689310.1:c.713G=
|
ENSP00000510438.1:p.Arg238=
|
|
ENST00000370818.8:c.761G=
MANE Select
|
ENSP00000359854.3:p.Arg254=
|
|
ENST00000394299.7:c.761G=
|
ENSP00000377836.2:p.Arg254=
|
|
ENST00000370818.7:c.761G=
|
ENSP00000359854.3:p.Arg254=
|
|
ENST00000394299.6:c.761G=
|
ENSP00000377836.2:p.Arg254=
|
|
ENST00000631057.2:c.599G=
|
ENSP00000486325.1:p.Arg200=
|
|
NM_001164617.1:c.761G=
|
NP_001158089.1:p.Arg254=
|
|
NM_001164618.1:c.713G=
|
NP_001158090.1:p.Arg238=
|
|
NM_001164619.1:c.599G=
|
NP_001158091.1:p.Arg200=
|
|
NM_004484.3:c.761G= , LRG_505t1:c.761G=
|
NP_004475.1:p.Arg254=
|
|
XM_017029413.2:c.761G=
|
XP_016884902.1:p.Arg254=
|
|
NM_001164617.2:c.761G=
|
NP_001158089.1:p.Arg254=
|
|
NM_001164618.2:c.713G=
|
NP_001158090.1:p.Arg238=
|
|
NM_001164619.2:c.599G=
|
NP_001158091.1:p.Arg200=
|
|
NM_004484.4:c.761G=
MANE Select
|
NP_004475.1:p.Arg254=
|
|