ENST00000181839.10:c.2116G>T
MANE Select
|
ENSP00000181839.4:p.Asp706Tyr
|
|
ENST00000340829.10:c.2116G>T
|
ENSP00000340557.5:p.Asp706Tyr
|
|
ENST00000484589.2:c.668G>T
|
|
|
ENST00000642213.1:n.598G>T
|
|
|
ENST00000643859.1:c.1007G>T
|
|
|
ENST00000643915.1:c.430G>T
|
ENSP00000496187.1:p.Asp144Tyr
|
|
ENST00000645470.1:c.46G>T
|
ENSP00000495036.1:p.Asp16Tyr
|
|
ENST00000646039.1:c.1456G>T
|
ENSP00000494168.1:p.Asp486Tyr
|
|
ENST00000646437.1:c.750G>T
|
|
|
ENST00000647453.1:n.1185G>T
|
|
|
ENST00000647518.1:n.3953G>T
|
|
|
ENST00000181839.8:c.2116G>T
|
ENSP00000181839.4:p.Asp706Tyr
|
|
ENST00000340829.9:c.2116G>T
|
ENSP00000340557.5:p.Asp706Tyr
|
|
ENST00000484589.1:n.668G>T
|
|
|
ENST00000611390.1:c.274G>T
|
ENSP00000484610.1:p.Asp92Tyr
|
|
ENST00000613626.4:c.274G>T
|
ENSP00000480835.1:p.Asp92Tyr
|
|
NM_003718.4:c.2116G>T
|
NP_003709.3:p.Asp706Tyr
|
|
NM_031267.3:c.2116G>T
|
NP_112557.2:p.Asp706Tyr
|
|
XM_011515597.1:c.2116G>T
|
XP_011513899.1:p.Asp706Tyr
|
|
XM_011515598.1:c.2116G>T
|
XP_011513900.1:p.Asp706Tyr
|
|
XM_011515597.3:c.2116G>T
|
XP_011513899.1:p.Asp706Tyr
|
|
XM_017012750.2:c.2116G>T
|
XP_016868239.1:p.Asp706Tyr
|
|
XM_017012751.2:c.2116G>T
|
XP_016868240.1:p.Asp706Tyr
|
|
NM_003718.5:c.2116G>T
MANE Select
|
NP_003709.3:p.Asp706Tyr
|
|