ENST00000682422.1:n.792C>A
|
|
|
ENST00000682545.1:c.*217C>A
|
ENSP00000508402.1:n.*217C>A
|
|
ENST00000682887.1:c.1612C>A
|
ENSP00000506946.1:n.1612C>A
|
|
ENST00000683302.1:c.1142C>A
|
ENSP00000507885.1:p.Ser381Tyr
|
|
ENST00000683557.1:c.*43C>A
|
ENSP00000508029.1:n.*43C>A
|
|
ENST00000367282.6:c.1211C>A
MANE Select
|
ENSP00000356251.4:p.Ser404Tyr
|
|
ENST00000367282.5:c.1211C>A
|
ENSP00000356251.4:p.Ser404Tyr
|
|
NM_004767.3:c.1211C>A
|
NP_004758.3:p.Ser404Tyr
|
|
XM_011510158.1:c.650C>A
|
XP_011508460.1:p.Ser217Tyr
|
|
NM_004767.4:c.1211C>A
|
NP_004758.3:p.Ser404Tyr
|
|
XM_011510158.2:c.650C>A
|
XP_011508460.1:p.Ser217Tyr
|
|
NM_004767.5:c.1211C>A
MANE Select
|
NP_004758.3:p.Ser404Tyr
|
|