ENST00000482750.6:c.367C>T
|
ENSP00000421262.2:p.His123Tyr
|
|
ENST00000696903.1:n.418C>T
|
|
|
ENST00000374202.7:c.367C>T
MANE Select
|
ENSP00000363318.3:p.His123Tyr
|
|
ENST00000642473.1:n.731C>T
|
|
|
ENST00000644022.1:n.773C>T
|
|
|
ENST00000644708.1:n.773C>T
|
|
|
ENST00000644911.1:n.773C>T
|
|
|
ENST00000645266.1:c.367C>T
|
ENSP00000493734.1:p.His123Tyr
|
|
ENST00000645518.1:c.367C>T
|
ENSP00000493986.1:p.His123Tyr
|
|
ENST00000646106.1:c.367C>T
|
ENSP00000496437.1:p.His123Tyr
|
|
ENST00000646505.1:c.367C>T
|
ENSP00000496673.1:p.His123Tyr
|
|
ENST00000647492.1:c.367C>T
|
ENSP00000495340.1:p.His123Tyr
|
|
ENST00000276110.6:n.752C>T
|
|
|
ENST00000374188.7:c.-350C>T
|
ENSP00000363303.3:n.-350C>T
|
|
ENST00000374202.6:c.367C>T
|
ENSP00000363318.2:p.His123Tyr
|
|
ENST00000456850.6:c.24+834C>T
|
ENSP00000388967.2:n.24+834C>T
|
|
ENST00000464642.5:c.235C>T
|
ENSP00000425233.1:p.His79Tyr
|
|
ENST00000487883.1:c.331C>T
|
ENSP00000423966.1:p.His111Tyr
|
|
ENST00000512747.3:n.434C>T
|
|
|
NM_000206.2:c.367C>T , LRG_150t1:c.367C>T
|
NP_000197.1:p.His123Tyr
|
|
NM_000206.3:c.367C>T
MANE Select
|
NP_000197.1:p.His123Tyr
|
|