ENST00000394867.9:n.1831G>T
|
|
|
ENST00000688751.1:n.528G>T
|
|
|
ENST00000689792.1:n.1296G>T
|
|
|
ENST00000262948.10:c.*189G>T
MANE Select
|
ENSP00000262948.4:n.*189G>T
|
|
ENST00000262948.9:c.*189G>T
|
ENSP00000262948.3:n.*189G>T
|
|
ENST00000394867.8:c.*189G>T
|
ENSP00000378336.1:n.*189G>T
|
|
ENST00000600584.5:n.2841G>T
|
|
|
ENST00000601786.5:n.1693G>T
|
|
|
NM_030662.3:c.*189G>T , LRG_750t1:c.*189G>T
|
NP_109587.1:n.*189G>T
|
|
XM_006722799.2:c.*189G>T
|
XP_006722862.1:n.*189G>T
|
|
XM_011528133.1:c.*189G>T
|
XP_011526435.1:n.*189G>T
|
|
NM_030662.4:c.*189G>T
MANE Select
|
NP_109587.1:n.*189G>T
|
|