ENST00000337554.8:c.*141G>T
MANE Select
|
ENSP00000338004.3:n.*141G>T
|
|
ENST00000329563.8:c.*141G>T
|
ENSP00000328973.4:n.*141G>T
|
|
ENST00000337554.7:c.*141G>T
|
ENSP00000338004.3:n.*141G>T
|
|
ENST00000396265.4:c.*141G>T
|
ENSP00000379563.4:n.*141G>T
|
|
ENST00000583777.5:c.*141G>T
|
ENSP00000463495.1:n.*141G>T
|
|
NM_000714.5:c.*141G>T
|
NP_000705.2:n.*141G>T
|
|
NM_001256530.1:c.*141G>T
|
NP_001243459.1:n.*141G>T
|
|
NM_001256531.1:c.*141G>T
|
NP_001243460.1:n.*141G>T
|
|
NR_046308.1:n.560G>T
|
|
|
NM_000714.6:c.*141G>T
MANE Select
|
NP_000705.2:n.*141G>T
|
|
NR_046308.2:n.515G>T
|
|
|