ENST00000261208.8:c.855+179T>G
MANE Select
|
ENSP00000261208.3:n.855+179T>G
|
|
ENST00000261208.7:c.855+179T>G
|
ENSP00000261208.3:n.855+179T>G
|
|
ENST00000538703.5:c.855+179T>G
|
ENSP00000440861.1:n.855+179T>G
|
|
ENST00000541929.5:c.231+179T>G
|
ENSP00000446364.1:n.231+179T>G
|
|
ENST00000544080.6:c.*284+179T>G
|
ENSP00000439385.2:n.*284+179T>G
|
|
ENST00000546999.5:c.*284+179T>G
|
ENSP00000447675.1:n.*284+179T>G
|
|
ENST00000551562.1:n.115+179T>G
|
|
|
ENST00000552509.5:c.819+179T>G
|
ENSP00000450372.1:n.819+179T>G
|
|
NM_001258333.1:c.231+179T>G
|
NP_001245262.1:n.231+179T>G
|
|
NM_001258334.1:c.855+179T>G
|
NP_001245263.1:n.855+179T>G
|
|
NM_002108.3:c.855+179T>G
|
NP_002099.1:n.855+179T>G
|
|
XM_011538249.1:c.4-1974T>G
|
XP_011536551.1:n.4-1974T>G
|
|
XM_011538249.2:c.4-1974T>G
|
XP_011536551.1:n.4-1974T>G
|
|
XM_017019246.1:c.-448T>G
|
XP_016874735.1:n.-448T>G
|
|
NM_002108.4:c.855+179T>G
MANE Select
|
NP_002099.1:n.855+179T>G
|
|
NM_001258334.2:c.855+179T>G
|
NP_001245263.1:n.855+179T>G
|
|
NM_001258333.2:c.231+179T>G
|
NP_001245262.1:n.231+179T>G
|
|