|
NM_015161.3:c.112C>T
MANE Select
|
NP_055976.1:p.Arg38Ter
|
|
ENST00000304414.12:c.112C>T
MANE Select
|
ENSP00000306788.7:p.Arg38Ter
|
|
NM_001313858.1:c.25C>T
|
NP_001300787.1:p.Arg9Ter
|
|
NM_015161.1:c.112C>T
|
NP_055976.1:p.Arg38Ter
|
|
NM_015161.2:c.112C>T
|
NP_055976.1:p.Arg38Ter
|
|
ENST00000304414.11:c.112C>T
|
ENSP00000306788.7:p.Arg38Ter
|
|
ENST00000546206.6:c.25C>T
|
ENSP00000440048.2:p.Arg9Ter
|
|
ENST00000562234.2:c.112C>T
|
ENSP00000455341.2:p.Arg38Ter
|
|
ENST00000562819.5:c.112C>T
|
ENSP00000457372.1:p.Arg38Ter
|
|
ENST00000563861.5:c.112C>T
|
ENSP00000456596.1:p.Arg38Ter
|
|
ENST00000566391.1:n.218C>T
|
|
|
ENST00000567078.2:c.112C>T
|
ENSP00000454746.2:p.Arg38Ter
|
|
ENST00000567969.1:n.190C>T
|
|
|
ENST00000569976.5:n.194C>T
|
|