ENST00000375448.4:c.1455+43_1455+44delinsTG
MANE Select
|
ENSP00000364597.4:n.1455+43_1455+44delinsTG
|
|
ENST00000467001.1:n.356+43_356+44delinsTG
|
|
|
ENST00000487048.5:n.422+43_422+44delinsTG
|
|
|
NM_012387.2:c.1455+43_1455+44delinsTG
|
NP_036519.2:n.1455+43_1455+44delinsTG
|
|
XM_011541150.1:c.1269+43_1269+44delinsTG
|
XP_011539452.1:n.1269+43_1269+44delinsTG
|
|
XM_011541151.1:c.1156-187_1156-186delinsTG
|
XP_011539453.1:n.1156-187_1156-186delinsTG
|
|
XM_011541152.1:c.918+43_918+44delinsTG
|
XP_011539454.1:n.918+43_918+44delinsTG
|
|
XM_011541157.1:c.564+43_564+44delinsTG
|
XP_011539459.1:n.564+43_564+44delinsTG
|
|
NM_012387.3:c.1455+43_1455+44delinsTG
MANE Select
|
NP_036519.2:n.1455+43_1455+44delinsTG
|
|