ENST00000515683.6:c.232G=
(ADH1C)
MANE Select
|
ENSP00000426083.1:p.Gly78=
|
|
ENST00000639454.1:c.18+5625G=
(ADH1B)
|
ENSP00000491622.1:n.18+5625G=
|
|
ENST00000505942.2:n.301G=
(ADH1C)
|
|
|
ENST00000510055.5:c.112G=
(ADH1C)
|
ENSP00000478439.1:p.Gly38=
|
|
ENST00000511397.3:c.130G=
(ADH1C)
|
ENSP00000478545.1:p.Gly44=
|
|
ENST00000515683.5:c.232G=
(ADH1C)
|
ENSP00000426083.1:p.Gly78=
|
|
NM_000669.4:c.232G=
(ADH1C)
|
NP_000660.1:p.Gly78=
|
|
NR_133005.1:n.602G=
(ADH1C)
|
|
|
XM_011531588.1:c.130G=
(ADH1C)
|
XP_011529890.1:p.Gly44=
|
|
XM_011531589.1:c.112G=
(ADH1C)
|
XP_011529891.1:p.Gly38=
|
|
NM_000669.5:c.232G=
(ADH1C)
MANE Select
|
NP_000660.1:p.Gly78=
|
|
NR_133005.2:n.303G=
(ADH1C)
|
|
|