ENST00000261208.8:c.855+59C>T
MANE Select
|
ENSP00000261208.3:n.855+59C>T
|
|
ENST00000261208.7:c.855+59C>T
|
ENSP00000261208.3:n.855+59C>T
|
|
ENST00000538703.5:c.855+59C>T
|
ENSP00000440861.1:n.855+59C>T
|
|
ENST00000541929.5:c.231+59C>T
|
ENSP00000446364.1:n.231+59C>T
|
|
ENST00000544080.6:c.*284+59C>T
|
ENSP00000439385.2:n.*284+59C>T
|
|
ENST00000546999.5:c.*284+59C>T
|
ENSP00000447675.1:n.*284+59C>T
|
|
ENST00000549376.1:n.307C>T
|
|
|
ENST00000551562.1:n.115+59C>T
|
|
|
ENST00000552509.5:c.819+59C>T
|
ENSP00000450372.1:n.819+59C>T
|
|
NM_001258333.1:c.231+59C>T
|
NP_001245262.1:n.231+59C>T
|
|
NM_001258334.1:c.855+59C>T
|
NP_001245263.1:n.855+59C>T
|
|
NM_002108.3:c.855+59C>T
|
NP_002099.1:n.855+59C>T
|
|
XM_011538249.1:c.4-2094C>T
|
XP_011536551.1:n.4-2094C>T
|
|
XM_011538249.2:c.4-2094C>T
|
XP_011536551.1:n.4-2094C>T
|
|
XM_017019246.1:c.-568C>T
|
XP_016874735.1:n.-568C>T
|
|
NM_002108.4:c.855+59C>T
MANE Select
|
NP_002099.1:n.855+59C>T
|
|
NM_001258334.2:c.855+59C>T
|
NP_001245263.1:n.855+59C>T
|
|
NM_001258333.2:c.231+59C>T
|
NP_001245262.1:n.231+59C>T
|
|