ENST00000517867.2:n.517C>T
|
|
|
ENST00000523077.2:n.733C>T
|
|
|
ENST00000521374.6:c.234C>T
MANE Select
|
ENSP00000430947.2:p.Tyr78=
|
|
ENST00000434833.6:c.234C>T
|
ENSP00000403219.2:p.Tyr78=
|
|
ENST00000517685.5:c.234C>T
|
ENSP00000428978.1:p.Tyr78=
|
|
ENST00000517729.5:c.108C>T
|
ENSP00000430299.1:p.Tyr36=
|
|
ENST00000518753.5:c.406C>T
|
|
|
ENST00000521314.5:c.125C>T
|
ENSP00000429580.1:p.Thr42Met
|
|
ENST00000521374.5:c.234C>T
|
ENSP00000430947.1:p.Tyr78=
|
|
ENST00000521624.5:c.234C>T
|
ENSP00000428161.1:p.Tyr78=
|
|
ENST00000522023.1:n.301C>T
|
|
|
ENST00000522295.5:c.234C>T
|
ENSP00000427832.1:p.Tyr78=
|
|
ENST00000522870.5:n.453C>T
|
|
|
ENST00000523077.1:n.733C>T
|
|
|
ENST00000523562.5:c.234C>T
|
ENSP00000430631.1:p.Tyr78=
|
|
ENST00000580114.5:c.1199C>T
|
|
|
ENST00000584272.5:c.234C>T
|
ENSP00000463706.1:p.Tyr78=
|
|
NM_001040667.2:c.234C>T
|
NP_001035757.1:p.Tyr78=
|
|
NM_001538.3:c.234C>T
|
NP_001529.2:p.Tyr78=
|
|
NM_001040667.3:c.234C>T
|
NP_001035757.1:p.Tyr78=
|
|
NM_001374674.1:c.234C>T
|
NP_001361603.1:p.Tyr78=
|
|
NM_001374675.1:c.234C>T
MANE Select
|
NP_001361604.1:p.Tyr78=
|
|
NM_001538.4:c.234C>T
|
NP_001529.2:p.Tyr78=
|
|