ENST00000262593.10:c.*315A>C
MANE Select
|
ENSP00000262593.5:n.*315A>C
|
|
ENST00000262593.9:c.*315A>C
|
ENSP00000262593.5:n.*315A>C
|
|
ENST00000395939.5:c.*315A>C
|
ENSP00000379270.1:n.*315A>C
|
|
NM_018431.4:c.*315A>C
|
NP_060901.2:n.*315A>C
|
|
NM_177959.2:c.*315A>C
|
NP_808874.1:n.*315A>C
|
|
XM_011528903.1:c.*315A>C
|
XP_011527205.1:n.*315A>C
|
|
XM_011528904.1:c.*315A>C
|
XP_011527206.1:n.*315A>C
|
|
XM_024451946.1:c.*315A>C
|
XP_024307714.1:n.*315A>C
|
|
NM_018431.5:c.*315A>C
MANE Select
|
NP_060901.2:n.*315A>C
|
|
NM_177959.3:c.*315A>C
|
NP_808874.1:n.*315A>C
|
|