ENST00000449291.7:c.1486T>G
MANE Select
|
ENSP00000401508.2:p.Leu496Val
|
|
ENST00000340490.7:c.1486T>G
|
ENSP00000341136.3:p.Leu496Val
|
|
ENST00000426292.7:c.1447T>G
|
ENSP00000390949.3:p.Leu483Val
|
|
ENST00000435154.7:c.*110T>G
|
ENSP00000405670.3:n.*110T>G
|
|
ENST00000449291.6:c.1486T>G
|
ENSP00000401508.2:p.Leu496Val
|
|
ENST00000460623.5:c.425T>G
|
|
|
ENST00000464332.5:n.1030T>G
|
|
|
ENST00000498076.5:n.265T>G
|
|
|
ENST00000529179.1:n.270T>G
|
|
|
NM_001286829.1:c.1447T>G
|
NP_001273758.1:p.Leu483Val
|
|
NM_145201.5:c.1486T>G
|
NP_660202.3:p.Leu496Val
|
|
XM_011517377.1:c.1292-154T>G
|
XP_011515679.1:n.1292-154T>G
|
|
NM_001363145.1:c.1405T>G
|
NP_001350074.1:p.Leu469Val
|
|
NM_001363146.1:c.802T>G
|
NP_001350075.1:p.Leu268Val
|
|
XM_017013975.2:c.1705T>G
|
XP_016869464.1:p.Leu569Val
|
|
XM_017013976.2:c.1705T>G
|
XP_016869465.1:p.Leu569Val
|
|
XM_017013977.2:c.1405T>G
|
XP_016869466.1:p.Leu469Val
|
|
XM_017013978.2:c.1511-154T>G
|
XP_016869467.1:n.1511-154T>G
|
|
XM_017013979.2:c.802T>G
|
XP_016869468.1:p.Leu268Val
|
|
XM_024447332.1:c.929-154T>G
|
XP_024303100.1:n.929-154T>G
|
|
XM_024447333.1:c.721T>G
|
XP_024303101.1:p.Leu241Val
|
|
NM_145201.6:c.1486T>G
MANE Select
|
NP_660202.3:p.Leu496Val
|
|
NM_001286829.2:c.1447T>G
|
NP_001273758.1:p.Leu483Val
|
|