ENST00000482750.6:c.612T>C
|
ENSP00000421262.2:p.Tyr204=
|
|
ENST00000696903.1:n.663T>C
|
|
|
ENST00000374202.7:c.612T>C
MANE Select
|
ENSP00000363318.3:p.Tyr204=
|
|
ENST00000642473.1:n.976T>C
|
|
|
ENST00000644022.1:n.878T>C
|
|
|
ENST00000644708.1:n.1018T>C
|
|
|
ENST00000644911.1:n.1018T>C
|
|
|
ENST00000645266.1:c.612T>C
|
ENSP00000493734.1:p.Tyr204=
|
|
ENST00000645518.1:c.612T>C
|
ENSP00000493986.1:p.Tyr204=
|
|
ENST00000646106.1:c.612T>C
|
ENSP00000496437.1:p.Tyr204=
|
|
ENST00000646505.1:c.612T>C
|
ENSP00000496673.1:p.Tyr204=
|
|
ENST00000647492.1:c.612T>C
|
ENSP00000495340.1:p.Tyr204=
|
|
ENST00000276110.6:n.1205T>C
|
|
|
ENST00000374188.7:c.-105T>C
|
ENSP00000363303.3:n.-105T>C
|
|
ENST00000374202.6:c.612T>C
|
ENSP00000363318.2:p.Tyr204=
|
|
ENST00000456850.6:c.42T>C
|
ENSP00000388967.2:p.Tyr14=
|
|
ENST00000464642.5:c.480T>C
|
ENSP00000425233.1:p.Tyr160=
|
|
ENST00000482750.5:c.25T>C
|
|
|
ENST00000512747.3:n.539T>C
|
|
|
NM_000206.2:c.612T>C , LRG_150t1:c.612T>C
|
NP_000197.1:p.Tyr204=
|
|
NM_000206.3:c.612T>C
MANE Select
|
NP_000197.1:p.Tyr204=
|
|