ENST00000696666.1:n.328A>T
|
|
|
ENST00000704002.1:c.239A>T
|
ENSP00000515615.1:p.Asp80Val
|
|
ENST00000704003.1:c.*93A>T
|
ENSP00000515616.1:n.*93A>T
|
|
ENST00000348035.9:c.140A>T
MANE Select
|
ENSP00000258737.7:p.Asp47Val
|
|
ENST00000348035.8:c.140A>T
|
ENSP00000258737.7:p.Asp47Val
|
|
ENST00000356142.4:c.140A>T
|
ENSP00000348461.4:p.Asp47Val
|
|
ENST00000488373.5:n.371A>T
|
|
|
ENST00000497741.5:n.156A>T
|
|
|
NM_006908.4:c.140A>T
|
NP_008839.2:p.Asp47Val
|
|
NM_018890.3:c.140A>T
|
NP_061485.1:p.Asp47Val
|
|
NM_006908.5:c.140A>T
MANE Select
|
NP_008839.2:p.Asp47Val
|
|
NM_018890.4:c.140A>T
|
NP_061485.1:p.Asp47Val
|
|