ENST00000356141.9:c.1959A>G
MANE Select
|
ENSP00000348460.4:p.Ser653=
|
|
ENST00000551634.6:c.1968A>G
|
ENSP00000448373.2:p.Ser656=
|
|
ENST00000680362.1:c.1859A>G
|
|
|
ENST00000681323.1:c.793+2685A>G
|
|
|
ENST00000346562.6:c.1863A>G
|
ENSP00000319610.5:p.Ser621=
|
|
ENST00000356141.8:c.1959A>G
|
ENSP00000348460.4:p.Ser653=
|
|
ENST00000357798.9:c.1920A>G
|
ENSP00000350446.5:p.Ser640=
|
|
ENST00000548645.5:c.1869A>G
|
ENSP00000448916.1:p.Ser623=
|
|
ENST00000551492.5:c.1974A>G
|
ENSP00000450392.1:p.Ser658=
|
|
ENST00000551634.5:c.1881A>G
|
ENSP00000448373.1:p.Ser627=
|
|
NM_001164749.1:c.1959A>G
|
NP_001158221.1:p.Ser653=
|
|
NM_001165893.1:c.1869A>G
|
NP_001159365.1:p.Ser623=
|
|
NM_022123.2:c.1863A>G
|
NP_071406.1:p.Ser621=
|
|
NM_173159.2:c.1920A>G
|
NP_775182.1:p.Ser640=
|
|
XM_005267991.2:c.1980A>G
|
XP_005268048.1:p.Ser660=
|
|
XM_005267992.2:c.1974A>G
|
XP_005268049.1:p.Ser658=
|
|
XM_005267993.2:c.1920A>G
|
XP_005268050.1:p.Ser640=
|
|
XM_011537067.1:c.2010A>G
|
XP_011535369.1:p.Ser670=
|
|
XM_011537068.1:c.2001A>G
|
XP_011535370.1:p.Ser667=
|
|
XM_011537069.1:c.1971A>G
|
XP_011535371.1:p.Ser657=
|
|
XM_011537070.1:c.1914A>G
|
XP_011535372.1:p.Ser638=
|
|
XM_011537071.1:c.1881A>G
|
XP_011535373.1:p.Ser627=
|
|
XM_011537072.1:c.1860A>G
|
XP_011535374.1:p.Ser620=
|
|
XM_011537073.1:c.1653A>G
|
XP_011535375.1:p.Ser551=
|
|
XM_011537074.1:c.1653A>G
|
XP_011535376.1:p.Ser551=
|
|
XM_005267991.3:c.2067A>G
|
XP_005268048.2:p.Ser689=
|
|
XM_005267992.3:c.2061A>G
|
XP_005268049.2:p.Ser687=
|
|
XM_011537067.2:c.2010A>G
|
XP_011535369.1:p.Ser670=
|
|
XM_011537069.2:c.2058A>G
|
XP_011535371.2:p.Ser686=
|
|
XM_011537070.2:c.1914A>G
|
XP_011535372.1:p.Ser638=
|
|
XM_011537071.2:c.1968A>G
|
XP_011535373.2:p.Ser656=
|
|
XM_011537072.2:c.1860A>G
|
XP_011535374.1:p.Ser620=
|
|
XM_017021582.1:c.2118A>G
|
XP_016877071.1:p.Ser706=
|
|
XM_017021583.1:c.2109A>G
|
XP_016877072.1:p.Ser703=
|
|
XM_017021584.1:c.2028A>G
|
XP_016877073.1:p.Ser676=
|
|
XM_017021585.1:c.1977A>G
|
XP_016877074.1:p.Ser659=
|
|
XM_017021586.1:c.1653A>G
|
XP_016877075.1:p.Ser551=
|
|
XM_017021587.1:c.1653A>G
|
XP_016877076.1:p.Ser551=
|
|
XM_017021588.1:c.1653A>G
|
XP_016877077.1:p.Ser551=
|
|
NM_001164749.2:c.1959A>G
MANE Select
|
NP_001158221.1:p.Ser653=
|
|
NM_001165893.2:c.1869A>G
|
NP_001159365.1:p.Ser623=
|
|
NM_022123.3:c.1863A>G
|
NP_071406.1:p.Ser621=
|
|
NM_173159.3:c.1920A>G
|
NP_775182.1:p.Ser640=
|
|
NM_001394988.1:c.1914A>G
|
NP_001381917.1:p.Ser638=
|
|
NM_001394989.1:c.1860A>G
|
NP_001381918.1:p.Ser620=
|
|