ENST00000360507.10:c.916C>T
MANE Select
|
ENSP00000353698.5:p.Arg306Trp
|
|
ENST00000360507.9:c.916C>T
|
ENSP00000353698.5:p.Arg306Trp
|
|
ENST00000409789.5:c.916C>T
|
ENSP00000386277.1:p.Arg306Trp
|
|
ENST00000453038.5:c.916C>T
|
ENSP00000410109.1:p.Arg306Trp
|
|
NM_015680.4:c.916C>T
|
NP_056495.3:p.Arg306Trp
|
|
XM_005246462.2:c.916C>T
|
XP_005246519.1:p.Arg306Trp
|
|
XM_005246463.3:c.916C>T
|
XP_005246520.1:p.Arg306Trp
|
|
XM_006712419.1:c.916C>T
|
XP_006712482.1:p.Arg306Trp
|
|
NM_001321389.1:c.916C>T
|
NP_001308318.1:p.Arg306Trp
|
|
NM_001321390.1:c.916C>T
|
NP_001308319.1:p.Arg306Trp
|
|
NM_001321391.1:c.916C>T
|
NP_001308320.1:p.Arg306Trp
|
|
NM_015680.5:c.916C>T
|
NP_056495.3:p.Arg306Trp
|
|
NR_135628.1:n.961C>T
|
|
|
NR_135629.1:n.1019C>T
|
|
|
XM_024452790.1:c.946C>T
|
XP_024308558.1:p.Arg316Trp
|
|
NM_015680.6:c.916C>T
MANE Select
|
NP_056495.4:p.Arg306Trp
|
|
NM_001321390.2:c.916C>T
|
NP_001308319.2:p.Arg306Trp
|
|
NM_001321391.2:c.916C>T
|
NP_001308320.2:p.Arg306Trp
|
|
NR_135628.2:n.944C>T
|
|
|
NR_135629.2:n.951C>T
|
|
|
NM_001321389.2:c.916C>T
|
NP_001308318.2:p.Arg306Trp
|
|