ENST00000700485.1:n.170A>T
|
|
|
ENST00000700486.1:n.208A>T
|
|
|
ENST00000700487.1:n.176A>T
|
|
|
ENST00000181839.10:c.2434A>T
MANE Select
|
ENSP00000181839.4:p.Asn812Tyr
|
|
ENST00000340829.10:c.2434A>T
|
ENSP00000340557.5:p.Asn812Tyr
|
|
ENST00000484589.2:c.986A>T
|
|
|
ENST00000643859.1:c.1325A>T
|
|
|
ENST00000643915.1:c.748A>T
|
ENSP00000496187.1:p.Asn250Tyr
|
|
ENST00000645470.1:c.364A>T
|
ENSP00000495036.1:p.Asn122Tyr
|
|
ENST00000646039.1:c.1774A>T
|
ENSP00000494168.1:p.Asn592Tyr
|
|
ENST00000647453.1:n.1503A>T
|
|
|
ENST00000181839.8:c.2434A>T
|
ENSP00000181839.4:p.Asn812Tyr
|
|
ENST00000340829.9:c.2434A>T
|
ENSP00000340557.5:p.Asn812Tyr
|
|
ENST00000484589.1:n.986A>T
|
|
|
ENST00000611390.1:c.592A>T
|
ENSP00000484610.1:p.Asn198Tyr
|
|
ENST00000613626.4:c.592A>T
|
ENSP00000480835.1:p.Asn198Tyr
|
|
NM_003718.4:c.2434A>T
|
NP_003709.3:p.Asn812Tyr
|
|
NM_031267.3:c.2434A>T
|
NP_112557.2:p.Asn812Tyr
|
|
XM_011515597.1:c.2434A>T
|
XP_011513899.1:p.Asn812Tyr
|
|
XM_011515598.1:c.2434A>T
|
XP_011513900.1:p.Asn812Tyr
|
|
XM_011515597.3:c.2434A>T
|
XP_011513899.1:p.Asn812Tyr
|
|
XM_017012750.2:c.2434A>T
|
XP_016868239.1:p.Asn812Tyr
|
|
XM_017012751.2:c.2434A>T
|
XP_016868240.1:p.Asn812Tyr
|
|
NM_003718.5:c.2434A>T
MANE Select
|
NP_003709.3:p.Asn812Tyr
|
|