ENST00000482750.6:c.262C=
|
ENSP00000421262.2:p.His88=
|
|
ENST00000696903.1:n.313C=
|
|
|
ENST00000374202.7:c.262C=
MANE Select
|
ENSP00000363318.3:p.His88=
|
|
ENST00000642473.1:n.626C=
|
|
|
ENST00000644022.1:n.668C=
|
|
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ENST00000644708.1:n.668C=
|
|
|
ENST00000644911.1:n.668C=
|
|
|
ENST00000645266.1:c.262C=
|
ENSP00000493734.1:p.His88=
|
|
ENST00000645518.1:c.262C=
|
ENSP00000493986.1:p.His88=
|
|
ENST00000646106.1:c.262C=
|
ENSP00000496437.1:p.His88=
|
|
ENST00000646505.1:c.262C=
|
ENSP00000496673.1:p.His88=
|
|
ENST00000647492.1:c.262C=
|
ENSP00000495340.1:p.His88=
|
|
ENST00000276110.6:n.647C=
|
|
|
ENST00000374188.7:c.-455C=
|
ENSP00000363303.3:n.-455C=
|
|
ENST00000374202.6:c.262C=
|
ENSP00000363318.2:p.His88=
|
|
ENST00000456850.6:c.24+521C=
|
ENSP00000388967.2:n.24+521C=
|
|
ENST00000464642.5:c.130C=
|
ENSP00000425233.1:p.His44=
|
|
ENST00000473378.1:c.199C=
|
ENSP00000423601.1:p.His67=
|
|
ENST00000487883.1:c.226C=
|
ENSP00000423966.1:p.His76=
|
|
ENST00000512747.3:n.329C=
|
|
|
NM_000206.2:c.262C= , LRG_150t1:c.262C=
|
NP_000197.1:p.His88=
|
|
NM_000206.3:c.262C=
MANE Select
|
NP_000197.1:p.His88=
|
|