ENST00000389652.11:c.439-274G>T
|
ENSP00000374303.8:n.439-274G>T
|
|
ENST00000424120.6:c.439-274G>T
MANE Select
|
ENSP00000403465.1:n.439-274G>T
|
|
ENST00000503292.6:c.439-274G>T
|
ENSP00000421809.1:n.439-274G>T
|
|
ENST00000506643.5:c.292-274G>T
|
ENSP00000422931.2:n.292-274G>T
|
|
ENST00000512702.6:c.439-274G>T
|
ENSP00000422875.2:n.439-274G>T
|
|
ENST00000514450.3:c.439-274G>T
|
ENSP00000502062.1:n.439-274G>T
|
|
ENST00000634028.2:c.292-274G>T
|
ENSP00000488669.2:n.292-274G>T
|
|
ENST00000650860.2:c.292-274G>T
|
ENSP00000498775.1:n.292-274G>T
|
|
ENST00000651385.1:c.292-274G>T
|
ENSP00000499005.1:n.292-274G>T
|
|
ENST00000674945.1:c.292-274G>T
|
ENSP00000502333.1:n.292-274G>T
|
|
ENST00000676337.1:c.292-274G>T
|
ENSP00000501728.1:n.292-274G>T
|
|
ENST00000424120.5:c.439-274G>T
|
ENSP00000403465.1:n.439-274G>T
|
|
ENST00000503292.5:c.439-274G>T
|
ENSP00000421809.1:n.439-274G>T
|
|
ENST00000512702.5:c.439-274G>T
|
ENSP00000422875.1:n.439-274G>T
|
|
ENST00000513811.5:n.619-274G>T
|
|
|
ENST00000514450.2:n.594-274G>T
|
|
|
ENST00000634028.1:c.422-274G>T
|
ENSP00000488669.1:n.422-274G>T
|
|
NM_001080522.2:c.439-274G>T , LRG_697t1:c.439-274G>T
|
NP_001073991.2:n.439-274G>T
|
|
XM_005248177.1:c.439-274G>T
|
XP_005248234.1:n.439-274G>T
|
|
XM_011513869.1:c.439-274G>T
|
XP_011512171.1:n.439-274G>T
|
|
XM_011513870.1:c.439-274G>T
|
XP_011512172.1:n.439-274G>T
|
|
XM_011513871.1:c.292-274G>T
|
XP_011512173.1:n.292-274G>T
|
|
XM_011513872.1:c.439-274G>T
|
XP_011512174.1:n.439-274G>T
|
|
XM_011513873.1:c.439-274G>T
|
XP_011512175.1:n.439-274G>T
|
|
XM_011513872.3:c.439-274G>T
|
XP_011512174.1:n.439-274G>T
|
|
XM_017008482.1:c.292-274G>T
|
XP_016863971.1:n.292-274G>T
|
|
XR_001741296.1:n.639-274G>T
|
|
|
NM_001378615.1:c.439-274G>T
MANE Select
|
NP_001365544.1:n.439-274G>T
|
|
NM_001378617.1:c.292-274G>T
|
NP_001365546.1:n.292-274G>T
|
|