ENST00000449291.7:c.1560G>T
MANE Select
|
ENSP00000401508.2:p.Val520=
|
|
ENST00000340490.7:c.1645G>T
|
ENSP00000341136.3:p.Ala549Ser
|
|
ENST00000426292.7:c.1521G>T
|
ENSP00000390949.3:p.Val507=
|
|
ENST00000435154.7:c.*269G>T
|
ENSP00000405670.3:n.*269G>T
|
|
ENST00000449291.6:c.1560G>T
|
ENSP00000401508.2:p.Val520=
|
|
ENST00000460623.5:c.584G>T
|
|
|
ENST00000464332.5:n.1104G>T
|
|
|
ENST00000498076.5:n.339G>T
|
|
|
ENST00000529179.1:n.344G>T
|
|
|
NM_001286829.1:c.1521G>T
|
NP_001273758.1:p.Val507=
|
|
NM_145201.5:c.1560G>T
|
NP_660202.3:p.Val520=
|
|
XM_011517377.1:c.1297G>T
|
XP_011515679.1:p.Ala433Ser
|
|
NM_001363145.1:c.1479G>T
|
NP_001350074.1:p.Val493=
|
|
NM_001363146.1:c.876G>T
|
NP_001350075.1:p.Val292=
|
|
XM_017013975.2:c.1864G>T
|
XP_016869464.1:p.Ala622Ser
|
|
XM_017013976.2:c.1779G>T
|
XP_016869465.1:p.Val593=
|
|
XM_017013977.2:c.1564G>T
|
XP_016869466.1:p.Ala522Ser
|
|
XM_017013978.2:c.1516G>T
|
XP_016869467.1:p.Ala506Ser
|
|
XM_017013979.2:c.961G>T
|
XP_016869468.1:p.Ala321Ser
|
|
XM_024447332.1:c.934G>T
|
XP_024303100.1:p.Ala312Ser
|
|
XM_024447333.1:c.880G>T
|
XP_024303101.1:p.Ala294Ser
|
|
NM_145201.6:c.1560G>T
MANE Select
|
NP_660202.3:p.Val520=
|
|
NM_001286829.2:c.1521G>T
|
NP_001273758.1:p.Val507=
|
|