ENST00000685279.1:c.*3539T>C
|
ENSP00000509424.1:n.*3539T>C
|
|
ENST00000692089.1:c.3399+5188T>C
|
ENSP00000508626.1:n.3399+5188T>C
|
|
ENST00000402219.8:c.*3539T>C
MANE Select
|
ENSP00000384675.2:n.*3539T>C
|
|
ENST00000402219.6:c.*3539T>C
|
ENSP00000384675.2:n.*3539T>C
|
|
ENST00000426016.5:c.*3539T>C
|
ENSP00000387784.1:n.*3539T>C
|
|
NM_005633.3:c.*3539T>C , LRG_754t1:c.*3539T>C
|
NP_005624.2:n.*3539T>C
|
|
XM_005264515.3:c.*3539T>C
|
XP_005264572.1:n.*3539T>C
|
|
XM_011533060.1:c.*3539T>C
|
XP_011531362.1:n.*3539T>C
|
|
XM_011533061.1:c.*3539T>C
|
XP_011531363.1:n.*3539T>C
|
|
XM_011533062.1:c.*3539T>C
|
XP_011531364.1:n.*3539T>C
|
|
XM_011533063.1:c.*3539T>C
|
XP_011531365.1:n.*3539T>C
|
|
XM_011533064.1:c.*3539T>C
|
XP_011531366.1:n.*3539T>C
|
|
XM_011533065.1:c.*3025T>C
|
XP_011531367.1:n.*3025T>C
|
|
XM_011533066.1:c.*3539T>C
|
XP_011531368.1:n.*3539T>C
|
|
NM_001382394.1:c.*3539T>C
|
NP_001369323.1:n.*3539T>C
|
|
NM_001382395.1:c.*3539T>C
|
NP_001369324.1:n.*3539T>C
|
|
NM_005633.4:c.*3539T>C
MANE Select
|
NP_005624.2:n.*3539T>C
|
|