ENST00000394867.9:n.1607A>T
|
|
|
ENST00000688002.1:n.3319A>T
|
|
|
ENST00000688751.1:n.304A>T
|
|
|
ENST00000689792.1:n.1072A>T
|
|
|
ENST00000262948.10:c.1168A>T
MANE Select
|
ENSP00000262948.4:p.Asn390Tyr
|
|
ENST00000262948.9:c.1168A>T
|
ENSP00000262948.3:p.Asn390Tyr
|
|
ENST00000394867.8:c.877A>T
|
ENSP00000378336.1:p.Asn293Tyr
|
|
ENST00000597263.5:n.353A>T
|
|
|
ENST00000599021.1:c.278A>T
|
|
|
ENST00000600584.5:n.2617A>T
|
|
|
ENST00000601786.5:n.1469A>T
|
|
|
NM_030662.3:c.1168A>T , LRG_750t1:c.1168A>T
|
NP_109587.1:p.Asn390Tyr
|
|
XM_006722799.2:c.889A>T
|
XP_006722862.1:p.Asn297Tyr
|
|
XM_011528133.1:c.598A>T
|
XP_011526435.1:p.Asn200Tyr
|
|
NM_030662.4:c.1168A>T
MANE Select
|
NP_109587.1:p.Asn390Tyr
|
|