ENST00000547400.6:c.-102G>T
|
ENSP00000446724.2:n.-102G>T
|
|
ENST00000551576.6:c.-5-139G>T
|
ENSP00000455848.2:n.-5-139G>T
|
|
ENST00000552678.2:c.-5-139G>T
|
ENSP00000457394.2:n.-5-139G>T
|
|
ENST00000388922.9:c.-5-139G>T
MANE Select
|
ENSP00000373574.4:n.-5-139G>T
|
|
ENST00000388922.8:c.-5-139G>T
|
ENSP00000373574.4:n.-5-139G>T
|
|
ENST00000547400.5:c.-102G>T
|
ENSP00000446724.1:n.-102G>T
|
|
ENST00000551576.5:c.-5-139G>T
|
ENSP00000455848.1:n.-5-139G>T
|
|
NM_000020.2:c.-5-139G>T , LRG_543t1:c.-5-139G>T
|
NP_000011.2:n.-5-139G>T
|
|
NM_001077401.1:c.-144G>T
|
NP_001070869.1:n.-144G>T
|
|
XM_005269235.2:c.-5-139G>T
|
XP_005269292.1:n.-5-139G>T
|
|
NM_000020.3:c.-5-139G>T
MANE Select
|
NP_000011.2:n.-5-139G>T
|
|