ENST00000358465.7:c.*2095G>A
MANE Select
|
ENSP00000351250.2:n.*2095G>A
|
|
ENST00000358465.6:c.*2095G>A
|
ENSP00000351250.2:n.*2095G>A
|
|
NM_015906.3:c.*2095G>A
|
NP_056990.3:n.*2095G>A
|
|
NM_033020.2:c.*2095G>A
|
NP_148980.2:n.*2095G>A
|
|
XM_005270936.2:c.*2095G>A
|
XP_005270993.1:n.*2095G>A
|
|
XM_005270937.2:c.*2095G>A
|
XP_005270994.1:n.*2095G>A
|
|
XM_011541568.1:c.*2095G>A
|
XP_011539870.1:n.*2095G>A
|
|
XM_005270936.4:c.*2095G>A
|
XP_005270993.1:n.*2095G>A
|
|
XM_005270937.4:c.*2095G>A
|
XP_005270994.1:n.*2095G>A
|
|
XM_011541568.3:c.*2095G>A
|
XP_011539870.1:n.*2095G>A
|
|
NM_015906.4:c.*2095G>A
MANE Select
|
NP_056990.3:n.*2095G>A
|
|
NM_033020.3:c.*2095G>A
|
NP_148980.2:n.*2095G>A
|
|