ENST00000584322.2:c.2334T>G
|
ENSP00000463272.2:p.Ala778=
|
|
ENST00000682066.1:c.2464T>G
|
ENSP00000507191.1:n.2464T>G
|
|
ENST00000682073.1:n.1074T>G
|
|
|
ENST00000682433.1:n.1413T>G
|
|
|
ENST00000682453.1:c.2334T>G
|
ENSP00000506943.1:p.Ala778=
|
|
ENST00000682477.1:c.*1760T>G
|
ENSP00000507075.1:n.*1760T>G
|
|
ENST00000682589.1:n.8211T>G
|
|
|
ENST00000682755.1:c.2112T>G
|
ENSP00000507660.1:p.Ala704=
|
|
ENST00000682989.1:c.2334T>G
|
ENSP00000507786.1:p.Ala778=
|
|
ENST00000683039.1:c.2334T>G
|
ENSP00000508303.1:p.Ala778=
|
|
ENST00000683235.1:c.2334T>G
|
ENSP00000507646.1:p.Ala778=
|
|
ENST00000683381.1:c.2394T>G
|
ENSP00000508184.1:p.Ala798=
|
|
ENST00000683535.1:n.464T>G
|
|
|
ENST00000684471.1:n.747T>G
|
|
|
ENST00000684584.1:c.1827T>G
|
ENSP00000508044.1:p.Ala609=
|
|
ENST00000684769.1:c.399T>G
|
ENSP00000507691.1:p.Ala133=
|
|
ENST00000259008.7:c.2334T>G
MANE Select
|
ENSP00000259008.2:p.Ala778=
|
|
ENST00000259008.6:c.2334T>G
|
ENSP00000259008.2:p.Ala778=
|
|
ENST00000577598.5:c.2334T>G
|
ENSP00000464654.1:p.Ala778=
|
|
ENST00000584322.1:c.317T>G
|
|
|
NM_032043.2:c.2334T>G , LRG_300t1:c.2334T>G
|
NP_114432.2:p.Ala778=
|
|
XM_011525332.1:c.2394T>G
|
XP_011523634.1:p.Ala798=
|
|
XM_011525333.1:c.2394T>G
|
XP_011523635.1:p.Ala798=
|
|
XM_011525334.1:c.2394T>G
|
XP_011523636.1:p.Ala798=
|
|
XM_011525335.1:c.2334T>G
|
XP_011523637.1:p.Ala778=
|
|
XM_011525336.1:c.2274T>G
|
XP_011523638.1:p.Ala758=
|
|
XM_011525337.1:c.2193T>G
|
XP_011523639.1:p.Ala731=
|
|
XM_011525338.1:c.1911T>G
|
XP_011523640.1:p.Ala637=
|
|
XM_011525339.1:c.2394T>G
|
XP_011523641.1:p.Ala798=
|
|
XM_011525340.1:c.2394T>G
|
XP_011523642.1:p.Ala798=
|
|
XR_934894.1:n.524-1123A>C
|
|
|
XM_011525332.3:c.2394T>G
|
XP_011523634.1:p.Ala798=
|
|
XM_011525333.3:c.2394T>G
|
XP_011523635.1:p.Ala798=
|
|
XM_011525334.2:c.2394T>G
|
XP_011523636.1:p.Ala798=
|
|
XM_011525335.3:c.2334T>G
|
XP_011523637.1:p.Ala778=
|
|
XM_011525336.2:c.2274T>G
|
XP_011523638.1:p.Ala758=
|
|
XM_011525337.2:c.2193T>G
|
XP_011523639.1:p.Ala731=
|
|
XM_011525338.2:c.1911T>G
|
XP_011523640.1:p.Ala637=
|
|
XM_011525339.3:c.2394T>G
|
XP_011523641.1:p.Ala798=
|
|
XM_011525340.3:c.2394T>G
|
XP_011523642.1:p.Ala798=
|
|
XM_017025200.1:c.1851T>G
|
XP_016880689.1:p.Ala617=
|
|
XM_017025201.1:c.1851T>G
|
XP_016880690.1:p.Ala617=
|
|
XM_017025202.1:c.480T>G
|
XP_016880691.1:p.Ala160=
|
|
XM_017025203.1:c.480T>G
|
XP_016880692.1:p.Ala160=
|
|
NM_032043.3:c.2334T>G
MANE Select
|
NP_114432.2:p.Ala778=
|
|