ENST00000181839.10:c.2176G>T
MANE Select
|
ENSP00000181839.4:p.Asp726Tyr
|
|
ENST00000340829.10:c.2176G>T
|
ENSP00000340557.5:p.Asp726Tyr
|
|
ENST00000484589.2:c.728G>T
|
|
|
ENST00000642213.1:n.658G>T
|
|
|
ENST00000643859.1:c.1067G>T
|
|
|
ENST00000643915.1:c.490G>T
|
ENSP00000496187.1:p.Asp164Tyr
|
|
ENST00000645470.1:c.106G>T
|
ENSP00000495036.1:p.Asp36Tyr
|
|
ENST00000646039.1:c.1516G>T
|
ENSP00000494168.1:p.Asp506Tyr
|
|
ENST00000647453.1:n.1245G>T
|
|
|
ENST00000647518.1:n.4013G>T
|
|
|
ENST00000181839.8:c.2176G>T
|
ENSP00000181839.4:p.Asp726Tyr
|
|
ENST00000340829.9:c.2176G>T
|
ENSP00000340557.5:p.Asp726Tyr
|
|
ENST00000484589.1:n.728G>T
|
|
|
ENST00000611390.1:c.334G>T
|
ENSP00000484610.1:p.Asp112Tyr
|
|
ENST00000613626.4:c.334G>T
|
ENSP00000480835.1:p.Asp112Tyr
|
|
NM_003718.4:c.2176G>T
|
NP_003709.3:p.Asp726Tyr
|
|
NM_031267.3:c.2176G>T
|
NP_112557.2:p.Asp726Tyr
|
|
XM_011515597.1:c.2176G>T
|
XP_011513899.1:p.Asp726Tyr
|
|
XM_011515598.1:c.2176G>T
|
XP_011513900.1:p.Asp726Tyr
|
|
XM_011515597.3:c.2176G>T
|
XP_011513899.1:p.Asp726Tyr
|
|
XM_017012750.2:c.2176G>T
|
XP_016868239.1:p.Asp726Tyr
|
|
XM_017012751.2:c.2176G>T
|
XP_016868240.1:p.Asp726Tyr
|
|
NM_003718.5:c.2176G>T
MANE Select
|
NP_003709.3:p.Asp726Tyr
|
|