NM_001170535.3:c.817C>T
MANE Select
|
NP_001164006.1:p.Arg273Cys
|
ENST00000378756.8:c.817C>T
MANE Select
|
ENSP00000368031.3:p.Arg273Cys
|
NM_001170535.1:c.817C>T
|
NP_001164006.1:p.Arg273Cys
|
NM_001170535.2:c.817C>T
|
NP_001164006.1:p.Arg273Cys
|
NM_001170536.1:c.580C>T
|
NP_001164007.1:p.Arg194Cys
|
NM_001170536.2:c.580C>T
|
NP_001164007.1:p.Arg194Cys
|
NM_001170536.3:c.580C>T
|
NP_001164007.1:p.Arg194Cys
|
NM_018188.3:c.961C>T
|
NP_060658.3:p.Arg321Cys
|
NM_018188.4:c.961C>T
|
NP_060658.3:p.Arg321Cys
|
NM_018188.5:c.961C>T
|
NP_060658.3:p.Arg321Cys
|
ENST00000339113.8:c.773C>T
|
|
ENST00000339113.9:c.781C>T
|
|
ENST00000378755.9:c.961C>T
|
ENSP00000368030.5:p.Arg321Cys
|
ENST00000378756.7:c.817C>T
|
ENSP00000368031.3:p.Arg273Cys
|
ENST00000536055.5:c.580C>T
|
ENSP00000439290.1:p.Arg194Cys
|
ENST00000536055.6:c.580C>T
|
ENSP00000439290.1:p.Arg194Cys
|
ENST00000672388.1:n.1154C>T
|
|
XM_024448098.1:c.817C>T
|
XP_024303866.1:p.Arg273Cys
|
XR_001737282.1:n.943C>T
|
|
XR_002956997.1:n.943C>T
|
|