ENST00000449291.7:c.1572G>T
MANE Select
|
ENSP00000401508.2:p.Arg524Ser
|
|
ENST00000340490.7:c.1657G>T
|
ENSP00000341136.3:p.Ala553Ser
|
|
ENST00000426292.7:c.1533G>T
|
ENSP00000390949.3:p.Arg511Ser
|
|
ENST00000435154.7:c.*281G>T
|
ENSP00000405670.3:n.*281G>T
|
|
ENST00000449291.6:c.1572G>T
|
ENSP00000401508.2:p.Arg524Ser
|
|
ENST00000460623.5:c.596G>T
|
|
|
ENST00000464332.5:n.1116G>T
|
|
|
ENST00000498076.5:n.351G>T
|
|
|
ENST00000529179.1:n.356G>T
|
|
|
NM_001286829.1:c.1533G>T
|
NP_001273758.1:p.Arg511Ser
|
|
NM_145201.5:c.1572G>T
|
NP_660202.3:p.Arg524Ser
|
|
XM_011517377.1:c.1309G>T
|
XP_011515679.1:p.Ala437Ser
|
|
NM_001363145.1:c.1491G>T
|
NP_001350074.1:p.Arg497Ser
|
|
NM_001363146.1:c.888G>T
|
NP_001350075.1:p.Arg296Ser
|
|
XM_017013975.2:c.1876G>T
|
XP_016869464.1:p.Ala626Ser
|
|
XM_017013976.2:c.1791G>T
|
XP_016869465.1:p.Arg597Ser
|
|
XM_017013977.2:c.1576G>T
|
XP_016869466.1:p.Ala526Ser
|
|
XM_017013978.2:c.1528G>T
|
XP_016869467.1:p.Ala510Ser
|
|
XM_017013979.2:c.973G>T
|
XP_016869468.1:p.Ala325Ser
|
|
XM_024447332.1:c.946G>T
|
XP_024303100.1:p.Ala316Ser
|
|
XM_024447333.1:c.892G>T
|
XP_024303101.1:p.Ala298Ser
|
|
NM_145201.6:c.1572G>T
MANE Select
|
NP_660202.3:p.Arg524Ser
|
|
NM_001286829.2:c.1533G>T
|
NP_001273758.1:p.Arg511Ser
|
|