|
ENST00000420682.7:c.1165G>T
|
ENSP00000413056.2:p.Asp389Tyr
|
|
|
ENST00000703922.1:c.1165G>T
|
ENSP00000515557.1:p.Asp389Tyr
|
|
|
ENST00000703923.1:c.1078G>T
|
ENSP00000515558.1:p.Asp360Tyr
|
|
|
ENST00000703924.1:c.1165G>T
|
ENSP00000515559.1:p.Asp389Tyr
|
|
|
ENST00000703978.1:c.1252G>T
|
ENSP00000515600.1:p.Asp418Tyr
|
|
|
ENST00000703980.1:n.478G>T
|
|
|
|
ENST00000703981.1:n.436G>T
|
|
|
|
ENST00000703982.1:n.670G>T
|
|
|
|
ENST00000262410.10:c.2428G>T
MANE Select
|
ENSP00000262410.6:p.Asp810Tyr
|
|
|
ENST00000344290.10:c.2137G>T
|
ENSP00000340820.6:p.Asp713Tyr
|
|
|
ENST00000351559.10:c.1252G>T
|
ENSP00000303214.7:p.Asp418Tyr
|
|
|
ENST00000535772.6:c.1072G>T
|
ENSP00000443028.2:p.Asp358Tyr
|
|
|
ENST00000680542.1:c.1165G>T
|
ENSP00000505258.1:p.Asp389Tyr
|
|
|
ENST00000680674.1:c.1201G>T
|
ENSP00000505478.1:p.Asp401Tyr
|
|
|
ENST00000262410.9:c.2203G>T
|
ENSP00000262410.5:p.Asp735Tyr
|
|
|
ENST00000334239.12:c.985G>T
|
ENSP00000334886.8:p.Asp329Tyr
|
|
|
ENST00000340799.9:c.1165G>T
|
ENSP00000340438.5:p.Asp389Tyr
|
|
|
ENST00000344290.9:c.2257G>T
|
ENSP00000340820.5:p.Asp753Tyr
|
|
|
ENST00000351559.9:c.1252G>T
|
ENSP00000303214.7:p.Asp418Tyr
|
|
|
ENST00000415613.6:c.2257G>T
|
ENSP00000410838.2:p.Asp753Tyr
|
|
|
ENST00000420682.6:c.1165G>T
|
ENSP00000413056.2:p.Asp389Tyr
|
|
|
ENST00000431008.7:c.1159G>T
|
ENSP00000389250.3:p.Asp387Tyr
|
|
|
ENST00000446361.7:c.1078G>T
|
ENSP00000408975.3:p.Asp360Tyr
|
|
|
ENST00000535772.5:c.1159G>T
|
ENSP00000443028.1:p.Asp387Tyr
|
|
|
ENST00000571987.5:c.2203G>T
|
ENSP00000458742.1:p.Asp735Tyr
|
|
|
ENST00000574436.5:c.1252G>T
|
ENSP00000460965.1:p.Asp418Tyr
|
|
|
ENST00000576518.1:n.6444G>T
|
|
|
|
NM_001123066.3:c.2257G>T
|
NP_001116538.2:p.Asp753Tyr
|
|
|
NM_001123067.3:c.1165G>T
|
NP_001116539.1:p.Asp389Tyr
|
|
|
NM_001203251.1:c.1072G>T
|
NP_001190180.1:p.Asp358Tyr
|
|
|
NM_001203252.1:c.1159G>T
|
NP_001190181.1:p.Asp387Tyr
|
|
|
NM_005910.5:c.1252G>T
|
NP_005901.2:p.Asp418Tyr
|
|
|
NM_016834.4:c.1078G>T
|
NP_058518.1:p.Asp360Tyr
|
|
|
NM_016835.4:c.2203G>T
|
NP_058519.3:p.Asp735Tyr
|
|
|
NM_016841.4:c.985G>T
|
NP_058525.1:p.Asp329Tyr
|
|
|
XM_005257362.3:c.2515G>T
|
XP_005257419.1:p.Asp839Tyr
|
|
|
XM_005257364.3:c.2428G>T
|
XP_005257421.1:p.Asp810Tyr
|
|
|
XM_005257365.3:c.2422G>T
|
XP_005257422.1:p.Asp808Tyr
|
|
|
XM_005257366.2:c.2341G>T
|
XP_005257423.1:p.Asp781Tyr
|
|
|
XM_005257367.3:c.2317G>T
|
XP_005257424.1:p.Asp773Tyr
|
|
|
XM_005257368.3:c.2224G>T
|
XP_005257425.1:p.Asp742Tyr
|
|
|
XM_005257369.3:c.1450G>T
|
XP_005257426.1:p.Asp484Tyr
|
|
|
XM_005257370.3:c.1363G>T
|
XP_005257427.1:p.Asp455Tyr
|
|
|
XM_005257371.3:c.1276G>T
|
XP_005257428.1:p.Asp426Tyr
|
|
|
XM_005257362.4:c.2515G>T
|
XP_005257419.1:p.Asp839Tyr
|
|
|
XM_005257364.4:c.2428G>T
|
XP_005257421.1:p.Asp810Tyr
|
|
|
XM_005257365.4:c.2422G>T
|
XP_005257422.1:p.Asp808Tyr
|
|
|
XM_005257366.3:c.2341G>T
|
XP_005257423.1:p.Asp781Tyr
|
|
|
XM_005257367.4:c.2317G>T
|
XP_005257424.1:p.Asp773Tyr
|
|
|
XM_005257368.4:c.2224G>T
|
XP_005257425.1:p.Asp742Tyr
|
|
|
XM_005257369.4:c.1450G>T
|
XP_005257426.1:p.Asp484Tyr
|
|
|
XM_005257370.4:c.1363G>T
|
XP_005257427.1:p.Asp455Tyr
|
|
|
XM_005257371.4:c.1276G>T
|
XP_005257428.1:p.Asp426Tyr
|
|
|
NM_001203251.2:c.1072G>T
|
NP_001190180.1:p.Asp358Tyr
|
|
|
NM_001377265.1:c.2428G>T
MANE Select
|
NP_001364194.1:p.Asp810Tyr
|
|
|
NM_001377266.1:c.2137G>T
|
NP_001364195.1:p.Asp713Tyr
|
|
|
NM_001377267.1:c.772-1020G>T
|
NP_001364196.1:n.772-1020G>T
|
|
|
NM_001377268.1:c.985G>T
|
NP_001364197.1:p.Asp329Tyr
|
|
|
NM_016834.5:c.1078G>T
|
NP_058518.1:p.Asp360Tyr
|
|
|
NM_016841.5:c.985G>T
|
NP_058525.1:p.Asp329Tyr
|
|
|
NR_165166.1:n.1083G>T
|
|
|
|
NM_001123066.4:c.2257G>T
|
NP_001116538.2:p.Asp753Tyr
|
|
|
NM_001123067.4:c.1165G>T
|
NP_001116539.1:p.Asp389Tyr
|
|
|
NM_001203252.2:c.1159G>T
|
NP_001190181.1:p.Asp387Tyr
|
|
|
NM_005910.6:c.1252G>T
|
NP_005901.2:p.Asp418Tyr
|
|
|
NM_016835.5:c.2203G>T
|
NP_058519.3:p.Asp735Tyr
|
|
