ENST00000421267.6:c.353G>C
|
|
|
ENST00000448821.6:c.2313G>C
|
ENSP00000402902.2:p.Gln771His
|
|
ENST00000685871.1:c.2241G>C
|
ENSP00000509964.1:p.Gln747His
|
|
ENST00000686159.1:n.2352G>C
|
|
|
ENST00000686486.1:n.1483G>C
|
|
|
ENST00000687302.1:n.2427G>C
|
|
|
ENST00000687357.1:c.2166G>C
|
ENSP00000509549.1:p.Gln722His
|
|
ENST00000687625.1:n.1468G>C
|
|
|
ENST00000687787.1:c.2472G>C
|
ENSP00000509440.1:p.Gln824His
|
|
ENST00000688201.1:n.2270G>C
|
|
|
ENST00000688226.1:n.2245G>C
|
|
|
ENST00000688869.1:n.2619G>C
|
|
|
ENST00000689788.1:c.2107G>C
|
ENSP00000508973.1:n.2107G>C
|
|
ENST00000689898.1:c.2170G>C
|
ENSP00000509651.1:n.2170G>C
|
|
ENST00000690070.1:c.2397G>C
|
ENSP00000509654.1:p.Gln799His
|
|
ENST00000690267.1:c.2102G>C
|
ENSP00000510432.1:n.2102G>C
|
|
ENST00000690552.1:n.2174G>C
|
|
|
ENST00000691138.1:n.2102G>C
|
|
|
ENST00000691969.1:c.1813G>C
|
ENSP00000510244.1:n.1813G>C
|
|
ENST00000692232.1:n.3628G>C
|
|
|
ENST00000692233.1:c.2177G>C
|
ENSP00000509698.1:n.2177G>C
|
|
ENST00000692380.1:n.1468G>C
|
|
|
ENST00000692447.1:n.3429G>C
|
|
|
ENST00000693094.1:c.2313G>C
|
ENSP00000510161.1:p.Gln771His
|
|
ENST00000342694.7:c.2313G>C
MANE Select
|
ENSP00000341083.2:p.Gln771His
|
|
ENST00000342694.6:c.2313G>C
|
ENSP00000341083.2:p.Gln771His
|
|
ENST00000421267.5:c.353G>C
|
|
|
ENST00000447210.5:c.90G>C
|
ENSP00000393029.1:p.Gln30His
|
|
ENST00000464810.5:n.2313G>C
|
|
|
NM_003995.3:c.2313G>C
|
NP_003986.2:p.Gln771His
|
|
XM_005251478.3:c.2322G>C
|
XP_005251535.1:p.Gln774His
|
|
XM_005251479.3:c.1335G>C
|
XP_005251536.1:p.Gln445His
|
|
XM_006716778.2:c.2250G>C
|
XP_006716841.1:p.Gln750His
|
|
XM_011517889.1:c.1335G>C
|
XP_011516191.1:p.Gln445His
|
|
XM_011517890.1:c.1335G>C
|
XP_011516192.1:p.Gln445His
|
|
XM_011517891.1:c.1335G>C
|
XP_011516193.1:p.Gln445His
|
|
XM_011517892.1:c.1335G>C
|
XP_011516194.1:p.Gln445His
|
|
XM_011517893.1:c.1335G>C
|
XP_011516195.1:p.Gln445His
|
|
XM_011517894.1:c.1335G>C
|
XP_011516196.1:p.Gln445His
|
|
XM_011517895.1:c.918G>C
|
XP_011516197.1:p.Gln306His
|
|
XM_024447556.1:c.2481G>C
|
XP_024303324.1:p.Gln827His
|
|
XM_024447557.1:c.2472G>C
|
XP_024303325.1:p.Gln824His
|
|
XM_024447558.1:c.1494G>C
|
XP_024303326.1:p.Gln498His
|
|
XM_024447559.1:c.1077G>C
|
XP_024303327.1:p.Gln359His
|
|
XM_024447560.1:c.1068G>C
|
XP_024303328.1:p.Gln356His
|
|
XM_024447561.1:c.909G>C
|
XP_024303329.1:p.Gln303His
|
|
NM_003995.4:c.2313G>C
MANE Select
|
NP_003986.2:p.Gln771His
|
|
NM_001378923.1:c.2322G>C
|
NP_001365852.1:p.Gln774His
|
|