|
NM_032043.3:c.2995A>T
MANE Select
|
NP_114432.2:p.Arg999Ter
|
|
ENST00000259008.7:c.2995A>T
MANE Select
|
ENSP00000259008.2:p.Arg999Ter
|
|
NM_032043.2:c.2995A>T , LRG_300t1:c.2995A>T
|
NP_114432.2:p.Arg999Ter
|
|
ENST00000259008.6:c.2995A>T
|
ENSP00000259008.2:p.Arg999Ter
|
|
ENST00000682073.1:n.1735A>T
|
|
|
ENST00000682453.1:c.2995A>T
|
ENSP00000506943.1:p.Arg999Ter
|
|
ENST00000682477.1:c.*2421A>T
|
ENSP00000507075.1:n.*2421A>T
|
|
ENST00000682589.1:n.8872A>T
|
|
|
ENST00000682755.1:c.2773A>T
|
ENSP00000507660.1:p.Arg925Ter
|
|
ENST00000682989.1:c.*86A>T
|
ENSP00000507786.1:n.*86A>T
|
|
ENST00000683039.1:c.2995A>T
|
ENSP00000508303.1:p.Arg999Ter
|
|
ENST00000683235.1:c.*410A>T
|
ENSP00000507646.1:n.*410A>T
|
|
ENST00000683535.1:n.1125A>T
|
|
|
ENST00000684584.1:c.2158A>T
|
ENSP00000508044.1:p.Arg720Ter
|
|
ENST00000684626.1:n.1241A>T
|
|
|
ENST00000684769.1:c.1185A>T
|
ENSP00000507691.1:n.1185A>T
|
|
XM_011525332.1:c.3055A>T
|
XP_011523634.1:p.Arg1019Ter
|
|
XM_011525332.3:c.3055A>T
|
XP_011523634.1:p.Arg1019Ter
|
|
XM_011525333.1:c.3055A>T
|
XP_011523635.1:p.Arg1019Ter
|
|
XM_011525333.3:c.3055A>T
|
XP_011523635.1:p.Arg1019Ter
|
|
XM_011525334.1:c.3055A>T
|
XP_011523636.1:p.Arg1019Ter
|
|
XM_011525334.2:c.3055A>T
|
XP_011523636.1:p.Arg1019Ter
|
|
XM_011525335.1:c.2995A>T
|
XP_011523637.1:p.Arg999Ter
|
|
XM_011525335.3:c.2995A>T
|
XP_011523637.1:p.Arg999Ter
|
|
XM_011525336.1:c.2935A>T
|
XP_011523638.1:p.Arg979Ter
|
|
XM_011525336.2:c.2935A>T
|
XP_011523638.1:p.Arg979Ter
|
|
XM_011525337.1:c.2854A>T
|
XP_011523639.1:p.Arg952Ter
|
|
XM_011525337.2:c.2854A>T
|
XP_011523639.1:p.Arg952Ter
|
|
XM_011525338.1:c.2572A>T
|
XP_011523640.1:p.Arg858Ter
|
|
XM_011525338.2:c.2572A>T
|
XP_011523640.1:p.Arg858Ter
|
|
XM_017025200.1:c.2512A>T
|
XP_016880689.1:p.Arg838Ter
|
|
XM_017025201.1:c.2512A>T
|
XP_016880690.1:p.Arg838Ter
|
|
XM_017025202.1:c.1141A>T
|
XP_016880691.1:p.Arg381Ter
|
|
XM_017025203.1:c.1141A>T
|
XP_016880692.1:p.Arg381Ter
|
