ENST00000356141.9:c.1970A>G
MANE Select
|
ENSP00000348460.4:p.Asn657Ser
|
|
ENST00000551634.6:c.1979A>G
|
ENSP00000448373.2:p.Asn660Ser
|
|
ENST00000680362.1:c.1870A>G
|
|
|
ENST00000681323.1:c.793+2696A>G
|
|
|
ENST00000346562.6:c.1874A>G
|
ENSP00000319610.5:p.Asn625Ser
|
|
ENST00000356141.8:c.1970A>G
|
ENSP00000348460.4:p.Asn657Ser
|
|
ENST00000357798.9:c.1931A>G
|
ENSP00000350446.5:p.Asn644Ser
|
|
ENST00000548645.5:c.1880A>G
|
ENSP00000448916.1:p.Asn627Ser
|
|
ENST00000551492.5:c.1985A>G
|
ENSP00000450392.1:p.Asn662Ser
|
|
ENST00000551634.5:c.1892A>G
|
ENSP00000448373.1:p.Asn631Ser
|
|
NM_001164749.1:c.1970A>G
|
NP_001158221.1:p.Asn657Ser
|
|
NM_001165893.1:c.1880A>G
|
NP_001159365.1:p.Asn627Ser
|
|
NM_022123.2:c.1874A>G
|
NP_071406.1:p.Asn625Ser
|
|
NM_173159.2:c.1931A>G
|
NP_775182.1:p.Asn644Ser
|
|
XM_005267991.2:c.1991A>G
|
XP_005268048.1:p.Asn664Ser
|
|
XM_005267992.2:c.1985A>G
|
XP_005268049.1:p.Asn662Ser
|
|
XM_005267993.2:c.1931A>G
|
XP_005268050.1:p.Asn644Ser
|
|
XM_011537067.1:c.2021A>G
|
XP_011535369.1:p.Asn674Ser
|
|
XM_011537068.1:c.2012A>G
|
XP_011535370.1:p.Asn671Ser
|
|
XM_011537069.1:c.1982A>G
|
XP_011535371.1:p.Asn661Ser
|
|
XM_011537070.1:c.1925A>G
|
XP_011535372.1:p.Asn642Ser
|
|
XM_011537071.1:c.1892A>G
|
XP_011535373.1:p.Asn631Ser
|
|
XM_011537072.1:c.1871A>G
|
XP_011535374.1:p.Asn624Ser
|
|
XM_011537073.1:c.1664A>G
|
XP_011535375.1:p.Asn555Ser
|
|
XM_011537074.1:c.1664A>G
|
XP_011535376.1:p.Asn555Ser
|
|
XM_005267991.3:c.2078A>G
|
XP_005268048.2:p.Asn693Ser
|
|
XM_005267992.3:c.2072A>G
|
XP_005268049.2:p.Asn691Ser
|
|
XM_011537067.2:c.2021A>G
|
XP_011535369.1:p.Asn674Ser
|
|
XM_011537069.2:c.2069A>G
|
XP_011535371.2:p.Asn690Ser
|
|
XM_011537070.2:c.1925A>G
|
XP_011535372.1:p.Asn642Ser
|
|
XM_011537071.2:c.1979A>G
|
XP_011535373.2:p.Asn660Ser
|
|
XM_011537072.2:c.1871A>G
|
XP_011535374.1:p.Asn624Ser
|
|
XM_017021582.1:c.2129A>G
|
XP_016877071.1:p.Asn710Ser
|
|
XM_017021583.1:c.2120A>G
|
XP_016877072.1:p.Asn707Ser
|
|
XM_017021584.1:c.2039A>G
|
XP_016877073.1:p.Asn680Ser
|
|
XM_017021585.1:c.1988A>G
|
XP_016877074.1:p.Asn663Ser
|
|
XM_017021586.1:c.1664A>G
|
XP_016877075.1:p.Asn555Ser
|
|
XM_017021587.1:c.1664A>G
|
XP_016877076.1:p.Asn555Ser
|
|
XM_017021588.1:c.1664A>G
|
XP_016877077.1:p.Asn555Ser
|
|
NM_001164749.2:c.1970A>G
MANE Select
|
NP_001158221.1:p.Asn657Ser
|
|
NM_001165893.2:c.1880A>G
|
NP_001159365.1:p.Asn627Ser
|
|
NM_022123.3:c.1874A>G
|
NP_071406.1:p.Asn625Ser
|
|
NM_173159.3:c.1931A>G
|
NP_775182.1:p.Asn644Ser
|
|
NM_001394988.1:c.1925A>G
|
NP_001381917.1:p.Asn642Ser
|
|
NM_001394989.1:c.1871A>G
|
NP_001381918.1:p.Asn624Ser
|
|