ENST00000449291.7:c.1588A>T
MANE Select
|
ENSP00000401508.2:p.Asn530Tyr
|
|
ENST00000340490.7:c.1673A>T
|
ENSP00000341136.3:p.Glu558Val
|
|
ENST00000426292.7:c.1549A>T
|
ENSP00000390949.3:p.Asn517Tyr
|
|
ENST00000435154.7:c.*297A>T
|
ENSP00000405670.3:n.*297A>T
|
|
ENST00000449291.6:c.1588A>T
|
ENSP00000401508.2:p.Asn530Tyr
|
|
ENST00000460623.5:c.612A>T
|
|
|
ENST00000464332.5:n.1132A>T
|
|
|
ENST00000498076.5:n.367A>T
|
|
|
ENST00000529179.1:n.372A>T
|
|
|
NM_001286829.1:c.1549A>T
|
NP_001273758.1:p.Asn517Tyr
|
|
NM_145201.5:c.1588A>T
|
NP_660202.3:p.Asn530Tyr
|
|
XM_011517377.1:c.1325A>T
|
XP_011515679.1:p.Glu442Val
|
|
NM_001363145.1:c.1507A>T
|
NP_001350074.1:p.Asn503Tyr
|
|
NM_001363146.1:c.904A>T
|
NP_001350075.1:p.Asn302Tyr
|
|
XM_017013975.2:c.1892A>T
|
XP_016869464.1:p.Glu631Val
|
|
XM_017013976.2:c.1807A>T
|
XP_016869465.1:p.Asn603Tyr
|
|
XM_017013977.2:c.1592A>T
|
XP_016869466.1:p.Glu531Val
|
|
XM_017013978.2:c.1544A>T
|
XP_016869467.1:p.Glu515Val
|
|
XM_017013979.2:c.989A>T
|
XP_016869468.1:p.Glu330Val
|
|
XM_024447332.1:c.962A>T
|
XP_024303100.1:p.Glu321Val
|
|
XM_024447333.1:c.908A>T
|
XP_024303101.1:p.Glu303Val
|
|
NM_145201.6:c.1588A>T
MANE Select
|
NP_660202.3:p.Asn530Tyr
|
|
NM_001286829.2:c.1549A>T
|
NP_001273758.1:p.Asn517Tyr
|
|