ENST00000449291.7:c.1581C>T
MANE Select
|
ENSP00000401508.2:p.Ala527=
|
|
ENST00000340490.7:c.1666C>T
|
ENSP00000341136.3:p.Pro556Ser
|
|
ENST00000426292.7:c.1542C>T
|
ENSP00000390949.3:p.Ala514=
|
|
ENST00000435154.7:c.*290C>T
|
ENSP00000405670.3:n.*290C>T
|
|
ENST00000449291.6:c.1581C>T
|
ENSP00000401508.2:p.Ala527=
|
|
ENST00000460623.5:c.605C>T
|
|
|
ENST00000464332.5:n.1125C>T
|
|
|
ENST00000498076.5:n.360C>T
|
|
|
ENST00000529179.1:n.365C>T
|
|
|
NM_001286829.1:c.1542C>T
|
NP_001273758.1:p.Ala514=
|
|
NM_145201.5:c.1581C>T
|
NP_660202.3:p.Ala527=
|
|
XM_011517377.1:c.1318C>T
|
XP_011515679.1:p.Pro440Ser
|
|
NM_001363145.1:c.1500C>T
|
NP_001350074.1:p.Ala500=
|
|
NM_001363146.1:c.897C>T
|
NP_001350075.1:p.Ala299=
|
|
XM_017013975.2:c.1885C>T
|
XP_016869464.1:p.Pro629Ser
|
|
XM_017013976.2:c.1800C>T
|
XP_016869465.1:p.Ala600=
|
|
XM_017013977.2:c.1585C>T
|
XP_016869466.1:p.Pro529Ser
|
|
XM_017013978.2:c.1537C>T
|
XP_016869467.1:p.Pro513Ser
|
|
XM_017013979.2:c.982C>T
|
XP_016869468.1:p.Pro328Ser
|
|
XM_024447332.1:c.955C>T
|
XP_024303100.1:p.Pro319Ser
|
|
XM_024447333.1:c.901C>T
|
XP_024303101.1:p.Pro301Ser
|
|
NM_145201.6:c.1581C>T
MANE Select
|
NP_660202.3:p.Ala527=
|
|
NM_001286829.2:c.1542C>T
|
NP_001273758.1:p.Ala514=
|
|