ENST00000553106.6:c.1199+332T>G
MANE Select
|
ENSP00000448059.1:n.1199+332T>G
|
|
ENST00000307000.7:c.1184+332T>G
|
ENSP00000303500.2:n.1184+332T>G
|
|
ENST00000549247.6:n.958+332T>G
|
|
|
ENST00000551114.2:n.861+332T>G
|
|
|
ENST00000553106.5:c.1199+332T>G
|
ENSP00000448059.1:n.1199+332T>G
|
|
ENST00000635477.1:c.303+332T>G
|
|
|
ENST00000635528.1:n.714+332T>G
|
|
|
NM_000277.1:c.1199+332T>G
|
NP_000268.1:n.1199+332T>G
|
|
XM_011538422.1:c.1142+332T>G
|
XP_011536724.1:n.1142+332T>G
|
|
NM_000277.2:c.1199+332T>G
|
NP_000268.1:n.1199+332T>G
|
|
NM_001354304.1:c.1199+332T>G
|
NP_001341233.1:n.1199+332T>G
|
|
NM_000277.3:c.1199+332T>G
MANE Select
|
NP_000268.1:n.1199+332T>G
|
|
NM_001354304.2:c.1199+332T>G
|
NP_001341233.1:n.1199+332T>G
|
|