ENST00000356141.9:c.1846C>A
MANE Select
|
ENSP00000348460.4:p.Arg616Ser
|
|
ENST00000551634.6:c.1855C>A
|
ENSP00000448373.2:p.Arg619Ser
|
|
ENST00000680362.1:c.1746C>A
|
|
|
ENST00000681323.1:c.793+2572C>A
|
|
|
ENST00000346562.6:c.1750C>A
|
ENSP00000319610.5:p.Arg584Ser
|
|
ENST00000356141.8:c.1846C>A
|
ENSP00000348460.4:p.Arg616Ser
|
|
ENST00000357798.9:c.1807C>A
|
ENSP00000350446.5:p.Arg603Ser
|
|
ENST00000548645.5:c.1756C>A
|
ENSP00000448916.1:p.Arg586Ser
|
|
ENST00000551492.5:c.1861C>A
|
ENSP00000450392.1:p.Arg621Ser
|
|
ENST00000551634.5:c.1768C>A
|
ENSP00000448373.1:p.Arg590Ser
|
|
NM_001164749.1:c.1846C>A
|
NP_001158221.1:p.Arg616Ser
|
|
NM_001165893.1:c.1756C>A
|
NP_001159365.1:p.Arg586Ser
|
|
NM_022123.2:c.1750C>A
|
NP_071406.1:p.Arg584Ser
|
|
NM_173159.2:c.1807C>A
|
NP_775182.1:p.Arg603Ser
|
|
XM_005267991.2:c.1867C>A
|
XP_005268048.1:p.Arg623Ser
|
|
XM_005267992.2:c.1861C>A
|
XP_005268049.1:p.Arg621Ser
|
|
XM_005267993.2:c.1807C>A
|
XP_005268050.1:p.Arg603Ser
|
|
XM_011537067.1:c.1897C>A
|
XP_011535369.1:p.Arg633Ser
|
|
XM_011537068.1:c.1888C>A
|
XP_011535370.1:p.Arg630Ser
|
|
XM_011537069.1:c.1858C>A
|
XP_011535371.1:p.Arg620Ser
|
|
XM_011537070.1:c.1801C>A
|
XP_011535372.1:p.Arg601Ser
|
|
XM_011537071.1:c.1768C>A
|
XP_011535373.1:p.Arg590Ser
|
|
XM_011537072.1:c.1747C>A
|
XP_011535374.1:p.Arg583Ser
|
|
XM_011537073.1:c.1540C>A
|
XP_011535375.1:p.Arg514Ser
|
|
XM_011537074.1:c.1540C>A
|
XP_011535376.1:p.Arg514Ser
|
|
XM_005267991.3:c.1954C>A
|
XP_005268048.2:p.Arg652Ser
|
|
XM_005267992.3:c.1948C>A
|
XP_005268049.2:p.Arg650Ser
|
|
XM_011537067.2:c.1897C>A
|
XP_011535369.1:p.Arg633Ser
|
|
XM_011537069.2:c.1945C>A
|
XP_011535371.2:p.Arg649Ser
|
|
XM_011537070.2:c.1801C>A
|
XP_011535372.1:p.Arg601Ser
|
|
XM_011537071.2:c.1855C>A
|
XP_011535373.2:p.Arg619Ser
|
|
XM_011537072.2:c.1747C>A
|
XP_011535374.1:p.Arg583Ser
|
|
XM_017021582.1:c.2005C>A
|
XP_016877071.1:p.Arg669Ser
|
|
XM_017021583.1:c.1996C>A
|
XP_016877072.1:p.Arg666Ser
|
|
XM_017021584.1:c.1915C>A
|
XP_016877073.1:p.Arg639Ser
|
|
XM_017021585.1:c.1864C>A
|
XP_016877074.1:p.Arg622Ser
|
|
XM_017021586.1:c.1540C>A
|
XP_016877075.1:p.Arg514Ser
|
|
XM_017021587.1:c.1540C>A
|
XP_016877076.1:p.Arg514Ser
|
|
XM_017021588.1:c.1540C>A
|
XP_016877077.1:p.Arg514Ser
|
|
NM_001164749.2:c.1846C>A
MANE Select
|
NP_001158221.1:p.Arg616Ser
|
|
NM_001165893.2:c.1756C>A
|
NP_001159365.1:p.Arg586Ser
|
|
NM_022123.3:c.1750C>A
|
NP_071406.1:p.Arg584Ser
|
|
NM_173159.3:c.1807C>A
|
NP_775182.1:p.Arg603Ser
|
|
NM_001394988.1:c.1801C>A
|
NP_001381917.1:p.Arg601Ser
|
|
NM_001394989.1:c.1747C>A
|
NP_001381918.1:p.Arg583Ser
|
|