ENST00000682066.1:c.2975C>T
|
ENSP00000507191.1:n.2975C>T
|
|
ENST00000682073.1:n.1585C>T
|
|
|
ENST00000682433.1:n.1924C>T
|
|
|
ENST00000682453.1:c.2845C>T
|
ENSP00000506943.1:p.Pro949Ser
|
|
ENST00000682477.1:c.*2271C>T
|
ENSP00000507075.1:n.*2271C>T
|
|
ENST00000682589.1:n.8722C>T
|
|
|
ENST00000682755.1:c.2623C>T
|
ENSP00000507660.1:p.Pro875Ser
|
|
ENST00000682989.1:c.2610-1756C>T
|
ENSP00000507786.1:n.2610-1756C>T
|
|
ENST00000683039.1:c.2845C>T
|
ENSP00000508303.1:p.Pro949Ser
|
|
ENST00000683235.1:c.*260C>T
|
ENSP00000507646.1:n.*260C>T
|
|
ENST00000683535.1:n.975C>T
|
|
|
ENST00000684471.1:n.1258C>T
|
|
|
ENST00000684584.1:c.2069-1756C>T
|
ENSP00000508044.1:n.2069-1756C>T
|
|
ENST00000684626.1:n.1091C>T
|
|
|
ENST00000684769.1:c.1035C>T
|
ENSP00000507691.1:n.1035C>T
|
|
ENST00000259008.7:c.2845C>T
MANE Select
|
ENSP00000259008.2:p.Pro949Ser
|
|
ENST00000259008.6:c.2845C>T
|
ENSP00000259008.2:p.Pro949Ser
|
|
ENST00000577598.5:c.2845C>T
|
ENSP00000464654.1:p.Pro949Ser
|
|
NM_032043.2:c.2845C>T , LRG_300t1:c.2845C>T
|
NP_114432.2:p.Pro949Ser
|
|
XM_011525332.1:c.2905C>T
|
XP_011523634.1:p.Pro969Ser
|
|
XM_011525333.1:c.2905C>T
|
XP_011523635.1:p.Pro969Ser
|
|
XM_011525334.1:c.2905C>T
|
XP_011523636.1:p.Pro969Ser
|
|
XM_011525335.1:c.2845C>T
|
XP_011523637.1:p.Pro949Ser
|
|
XM_011525336.1:c.2785C>T
|
XP_011523638.1:p.Pro929Ser
|
|
XM_011525337.1:c.2704C>T
|
XP_011523639.1:p.Pro902Ser
|
|
XM_011525338.1:c.2422C>T
|
XP_011523640.1:p.Pro808Ser
|
|
XM_011525332.3:c.2905C>T
|
XP_011523634.1:p.Pro969Ser
|
|
XM_011525333.3:c.2905C>T
|
XP_011523635.1:p.Pro969Ser
|
|
XM_011525334.2:c.2905C>T
|
XP_011523636.1:p.Pro969Ser
|
|
XM_011525335.3:c.2845C>T
|
XP_011523637.1:p.Pro949Ser
|
|
XM_011525336.2:c.2785C>T
|
XP_011523638.1:p.Pro929Ser
|
|
XM_011525337.2:c.2704C>T
|
XP_011523639.1:p.Pro902Ser
|
|
XM_011525338.2:c.2422C>T
|
XP_011523640.1:p.Pro808Ser
|
|
XM_017025200.1:c.2362C>T
|
XP_016880689.1:p.Pro788Ser
|
|
XM_017025201.1:c.2362C>T
|
XP_016880690.1:p.Pro788Ser
|
|
XM_017025202.1:c.991C>T
|
XP_016880691.1:p.Pro331Ser
|
|
XM_017025203.1:c.991C>T
|
XP_016880692.1:p.Pro331Ser
|
|
NM_032043.3:c.2845C>T
MANE Select
|
NP_114432.2:p.Pro949Ser
|
|