ENST00000356141.9:c.1983C>G
MANE Select
|
ENSP00000348460.4:p.Asp661Glu
|
|
ENST00000551634.6:c.1992C>G
|
ENSP00000448373.2:p.Asp664Glu
|
|
ENST00000680362.1:c.1883C>G
|
|
|
ENST00000681323.1:c.793+2709C>G
|
|
|
ENST00000346562.6:c.1887C>G
|
ENSP00000319610.5:p.Asp629Glu
|
|
ENST00000356141.8:c.1983C>G
|
ENSP00000348460.4:p.Asp661Glu
|
|
ENST00000357798.9:c.1944C>G
|
ENSP00000350446.5:p.Asp648Glu
|
|
ENST00000548645.5:c.1893C>G
|
ENSP00000448916.1:p.Asp631Glu
|
|
ENST00000551492.5:c.1998C>G
|
ENSP00000450392.1:p.Asp666Glu
|
|
ENST00000551634.5:c.1905C>G
|
ENSP00000448373.1:p.Asp635Glu
|
|
NM_001164749.1:c.1983C>G
|
NP_001158221.1:p.Asp661Glu
|
|
NM_001165893.1:c.1893C>G
|
NP_001159365.1:p.Asp631Glu
|
|
NM_022123.2:c.1887C>G
|
NP_071406.1:p.Asp629Glu
|
|
NM_173159.2:c.1944C>G
|
NP_775182.1:p.Asp648Glu
|
|
XM_005267991.2:c.2004C>G
|
XP_005268048.1:p.Asp668Glu
|
|
XM_005267992.2:c.1998C>G
|
XP_005268049.1:p.Asp666Glu
|
|
XM_005267993.2:c.1944C>G
|
XP_005268050.1:p.Asp648Glu
|
|
XM_011537067.1:c.2034C>G
|
XP_011535369.1:p.Asp678Glu
|
|
XM_011537068.1:c.2025C>G
|
XP_011535370.1:p.Asp675Glu
|
|
XM_011537069.1:c.1995C>G
|
XP_011535371.1:p.Asp665Glu
|
|
XM_011537070.1:c.1938C>G
|
XP_011535372.1:p.Asp646Glu
|
|
XM_011537071.1:c.1905C>G
|
XP_011535373.1:p.Asp635Glu
|
|
XM_011537072.1:c.1884C>G
|
XP_011535374.1:p.Asp628Glu
|
|
XM_011537073.1:c.1677C>G
|
XP_011535375.1:p.Asp559Glu
|
|
XM_011537074.1:c.1677C>G
|
XP_011535376.1:p.Asp559Glu
|
|
XM_005267991.3:c.2091C>G
|
XP_005268048.2:p.Asp697Glu
|
|
XM_005267992.3:c.2085C>G
|
XP_005268049.2:p.Asp695Glu
|
|
XM_011537067.2:c.2034C>G
|
XP_011535369.1:p.Asp678Glu
|
|
XM_011537069.2:c.2082C>G
|
XP_011535371.2:p.Asp694Glu
|
|
XM_011537070.2:c.1938C>G
|
XP_011535372.1:p.Asp646Glu
|
|
XM_011537071.2:c.1992C>G
|
XP_011535373.2:p.Asp664Glu
|
|
XM_011537072.2:c.1884C>G
|
XP_011535374.1:p.Asp628Glu
|
|
XM_017021582.1:c.2142C>G
|
XP_016877071.1:p.Asp714Glu
|
|
XM_017021583.1:c.2133C>G
|
XP_016877072.1:p.Asp711Glu
|
|
XM_017021584.1:c.2052C>G
|
XP_016877073.1:p.Asp684Glu
|
|
XM_017021585.1:c.2001C>G
|
XP_016877074.1:p.Asp667Glu
|
|
XM_017021586.1:c.1677C>G
|
XP_016877075.1:p.Asp559Glu
|
|
XM_017021587.1:c.1677C>G
|
XP_016877076.1:p.Asp559Glu
|
|
XM_017021588.1:c.1677C>G
|
XP_016877077.1:p.Asp559Glu
|
|
NM_001164749.2:c.1983C>G
MANE Select
|
NP_001158221.1:p.Asp661Glu
|
|
NM_001165893.2:c.1893C>G
|
NP_001159365.1:p.Asp631Glu
|
|
NM_022123.3:c.1887C>G
|
NP_071406.1:p.Asp629Glu
|
|
NM_173159.3:c.1944C>G
|
NP_775182.1:p.Asp648Glu
|
|
NM_001394988.1:c.1938C>G
|
NP_001381917.1:p.Asp646Glu
|
|
NM_001394989.1:c.1884C>G
|
NP_001381918.1:p.Asp628Glu
|
|