ENST00000448821.6:c.1219-1G>A
|
ENSP00000402902.2:n.1219-1G>A
|
|
ENST00000685871.1:c.1219-1G>A
|
ENSP00000509964.1:n.1219-1G>A
|
|
ENST00000686159.1:n.1258-1G>A
|
|
|
ENST00000686486.1:n.226G>A
|
|
|
ENST00000687302.1:n.1304G>A
|
|
|
ENST00000687357.1:c.1219-1G>A
|
ENSP00000509549.1:n.1219-1G>A
|
|
ENST00000687625.1:n.374-1G>A
|
|
|
ENST00000687787.1:c.1219-1G>A
|
ENSP00000509440.1:n.1219-1G>A
|
|
ENST00000688201.1:n.1251-1G>A
|
|
|
ENST00000688226.1:n.1151-1G>A
|
|
|
ENST00000688869.1:n.1524G>A
|
|
|
ENST00000689788.1:c.1013-1G>A
|
ENSP00000508973.1:n.1013-1G>A
|
|
ENST00000689898.1:c.1219-1G>A
|
ENSP00000509651.1:n.1219-1G>A
|
|
ENST00000690070.1:c.1219-1G>A
|
ENSP00000509654.1:n.1219-1G>A
|
|
ENST00000690267.1:c.1083-1G>A
|
ENSP00000510432.1:n.1083-1G>A
|
|
ENST00000690552.1:n.1080-1G>A
|
|
|
ENST00000691138.1:n.1080-1G>A
|
|
|
ENST00000691969.1:c.794-1G>A
|
ENSP00000510244.1:n.794-1G>A
|
|
ENST00000692232.1:n.2374G>A
|
|
|
ENST00000692233.1:c.1083-1G>A
|
ENSP00000509698.1:n.1083-1G>A
|
|
ENST00000692380.1:n.374-1G>A
|
|
|
ENST00000692447.1:n.2331-1G>A
|
|
|
ENST00000693094.1:c.1219-1G>A
|
ENSP00000510161.1:n.1219-1G>A
|
|
ENST00000342694.7:c.1219-1G>A
MANE Select
|
ENSP00000341083.2:n.1219-1G>A
|
|
ENST00000342694.6:c.1219-1G>A
|
ENSP00000341083.2:n.1219-1G>A
|
|
ENST00000464810.5:n.1219-1G>A
|
|
|
NM_003995.3:c.1219-1G>A
|
NP_003986.2:n.1219-1G>A
|
|
XM_005251478.3:c.1219-1G>A
|
XP_005251535.1:n.1219-1G>A
|
|
XM_005251479.3:c.232-1G>A
|
XP_005251536.1:n.232-1G>A
|
|
XM_006716778.2:c.1219-1G>A
|
XP_006716841.1:n.1219-1G>A
|
|
XM_011517889.1:c.232-1G>A
|
XP_011516191.1:n.232-1G>A
|
|
XM_011517890.1:c.232-1G>A
|
XP_011516192.1:n.232-1G>A
|
|
XM_011517891.1:c.232-1G>A
|
XP_011516193.1:n.232-1G>A
|
|
XM_011517892.1:c.232-1G>A
|
XP_011516194.1:n.232-1G>A
|
|
XM_011517893.1:c.232-1G>A
|
XP_011516195.1:n.232-1G>A
|
|
XM_011517894.1:c.232-1G>A
|
XP_011516196.1:n.232-1G>A
|
|
XM_024447556.1:c.1219-1G>A
|
XP_024303324.1:n.1219-1G>A
|
|
XM_024447557.1:c.1219-1G>A
|
XP_024303325.1:n.1219-1G>A
|
|
XM_024447558.1:c.232-1G>A
|
XP_024303326.1:n.232-1G>A
|
|
XM_024447560.1:c.-190-1G>A
|
XP_024303328.1:n.-190-1G>A
|
|
XM_024447561.1:c.-190-1G>A
|
XP_024303329.1:n.-190-1G>A
|
|
NM_003995.4:c.1219-1G>A
MANE Select
|
NP_003986.2:n.1219-1G>A
|
|
NM_001378923.1:c.1219-1G>A
|
NP_001365852.1:n.1219-1G>A
|
|