ENST00000421267.6:c.351C=
|
|
|
ENST00000448821.6:c.2311C=
|
ENSP00000402902.2:p.Gln771=
|
|
ENST00000685871.1:c.2239C=
|
ENSP00000509964.1:p.Gln747=
|
|
ENST00000686159.1:n.2350C=
|
|
|
ENST00000686486.1:n.1481C=
|
|
|
ENST00000687302.1:n.2425C=
|
|
|
ENST00000687357.1:c.2164C=
|
ENSP00000509549.1:p.Gln722=
|
|
ENST00000687625.1:n.1466C=
|
|
|
ENST00000687787.1:c.2470C=
|
ENSP00000509440.1:p.Gln824=
|
|
ENST00000688201.1:n.2268C=
|
|
|
ENST00000688226.1:n.2243C=
|
|
|
ENST00000688869.1:n.2617C=
|
|
|
ENST00000689788.1:c.2105C=
|
ENSP00000508973.1:n.2105C=
|
|
ENST00000689898.1:c.2168C=
|
ENSP00000509651.1:n.2168C=
|
|
ENST00000690070.1:c.2395C=
|
ENSP00000509654.1:p.Gln799=
|
|
ENST00000690267.1:c.2100C=
|
ENSP00000510432.1:n.2100C=
|
|
ENST00000690552.1:n.2172C=
|
|
|
ENST00000691138.1:n.2100C=
|
|
|
ENST00000691969.1:c.1811C=
|
ENSP00000510244.1:n.1811C=
|
|
ENST00000692232.1:n.3626C=
|
|
|
ENST00000692233.1:c.2175C=
|
ENSP00000509698.1:n.2175C=
|
|
ENST00000692380.1:n.1466C=
|
|
|
ENST00000692447.1:n.3427C=
|
|
|
ENST00000693094.1:c.2311C=
|
ENSP00000510161.1:p.Gln771=
|
|
ENST00000342694.7:c.2311C=
MANE Select
|
ENSP00000341083.2:p.Gln771=
|
|
ENST00000342694.6:c.2311C=
|
ENSP00000341083.2:p.Gln771=
|
|
ENST00000421267.5:c.351C=
|
|
|
ENST00000447210.5:c.88C=
|
ENSP00000393029.1:p.Gln30=
|
|
ENST00000464810.5:n.2311C=
|
|
|
NM_003995.3:c.2311C=
|
NP_003986.2:p.Gln771=
|
|
XM_005251478.3:c.2320C=
|
XP_005251535.1:p.Gln774=
|
|
XM_005251479.3:c.1333C=
|
XP_005251536.1:p.Gln445=
|
|
XM_006716778.2:c.2248C=
|
XP_006716841.1:p.Gln750=
|
|
XM_011517889.1:c.1333C=
|
XP_011516191.1:p.Gln445=
|
|
XM_011517890.1:c.1333C=
|
XP_011516192.1:p.Gln445=
|
|
XM_011517891.1:c.1333C=
|
XP_011516193.1:p.Gln445=
|
|
XM_011517892.1:c.1333C=
|
XP_011516194.1:p.Gln445=
|
|
XM_011517893.1:c.1333C=
|
XP_011516195.1:p.Gln445=
|
|
XM_011517894.1:c.1333C=
|
XP_011516196.1:p.Gln445=
|
|
XM_011517895.1:c.916C=
|
XP_011516197.1:p.Gln306=
|
|
XM_024447556.1:c.2479C=
|
XP_024303324.1:p.Gln827=
|
|
XM_024447557.1:c.2470C=
|
XP_024303325.1:p.Gln824=
|
|
XM_024447558.1:c.1492C=
|
XP_024303326.1:p.Gln498=
|
|
XM_024447559.1:c.1075C=
|
XP_024303327.1:p.Gln359=
|
|
XM_024447560.1:c.1066C=
|
XP_024303328.1:p.Gln356=
|
|
XM_024447561.1:c.907C=
|
XP_024303329.1:p.Gln303=
|
|
NM_003995.4:c.2311C=
MANE Select
|
NP_003986.2:p.Gln771=
|
|
NM_001378923.1:c.2320C=
|
NP_001365852.1:p.Gln774=
|
|