ENST00000356141.9:c.1964C>G
MANE Select
|
ENSP00000348460.4:p.Pro655Arg
|
|
ENST00000551634.6:c.1973C>G
|
ENSP00000448373.2:p.Pro658Arg
|
|
ENST00000680362.1:c.1864C>G
|
|
|
ENST00000681323.1:c.793+2690C>G
|
|
|
ENST00000346562.6:c.1868C>G
|
ENSP00000319610.5:p.Pro623Arg
|
|
ENST00000356141.8:c.1964C>G
|
ENSP00000348460.4:p.Pro655Arg
|
|
ENST00000357798.9:c.1925C>G
|
ENSP00000350446.5:p.Pro642Arg
|
|
ENST00000548645.5:c.1874C>G
|
ENSP00000448916.1:p.Pro625Arg
|
|
ENST00000551492.5:c.1979C>G
|
ENSP00000450392.1:p.Pro660Arg
|
|
ENST00000551634.5:c.1886C>G
|
ENSP00000448373.1:p.Pro629Arg
|
|
NM_001164749.1:c.1964C>G
|
NP_001158221.1:p.Pro655Arg
|
|
NM_001165893.1:c.1874C>G
|
NP_001159365.1:p.Pro625Arg
|
|
NM_022123.2:c.1868C>G
|
NP_071406.1:p.Pro623Arg
|
|
NM_173159.2:c.1925C>G
|
NP_775182.1:p.Pro642Arg
|
|
XM_005267991.2:c.1985C>G
|
XP_005268048.1:p.Pro662Arg
|
|
XM_005267992.2:c.1979C>G
|
XP_005268049.1:p.Pro660Arg
|
|
XM_005267993.2:c.1925C>G
|
XP_005268050.1:p.Pro642Arg
|
|
XM_011537067.1:c.2015C>G
|
XP_011535369.1:p.Pro672Arg
|
|
XM_011537068.1:c.2006C>G
|
XP_011535370.1:p.Pro669Arg
|
|
XM_011537069.1:c.1976C>G
|
XP_011535371.1:p.Pro659Arg
|
|
XM_011537070.1:c.1919C>G
|
XP_011535372.1:p.Pro640Arg
|
|
XM_011537071.1:c.1886C>G
|
XP_011535373.1:p.Pro629Arg
|
|
XM_011537072.1:c.1865C>G
|
XP_011535374.1:p.Pro622Arg
|
|
XM_011537073.1:c.1658C>G
|
XP_011535375.1:p.Pro553Arg
|
|
XM_011537074.1:c.1658C>G
|
XP_011535376.1:p.Pro553Arg
|
|
XM_005267991.3:c.2072C>G
|
XP_005268048.2:p.Pro691Arg
|
|
XM_005267992.3:c.2066C>G
|
XP_005268049.2:p.Pro689Arg
|
|
XM_011537067.2:c.2015C>G
|
XP_011535369.1:p.Pro672Arg
|
|
XM_011537069.2:c.2063C>G
|
XP_011535371.2:p.Pro688Arg
|
|
XM_011537070.2:c.1919C>G
|
XP_011535372.1:p.Pro640Arg
|
|
XM_011537071.2:c.1973C>G
|
XP_011535373.2:p.Pro658Arg
|
|
XM_011537072.2:c.1865C>G
|
XP_011535374.1:p.Pro622Arg
|
|
XM_017021582.1:c.2123C>G
|
XP_016877071.1:p.Pro708Arg
|
|
XM_017021583.1:c.2114C>G
|
XP_016877072.1:p.Pro705Arg
|
|
XM_017021584.1:c.2033C>G
|
XP_016877073.1:p.Pro678Arg
|
|
XM_017021585.1:c.1982C>G
|
XP_016877074.1:p.Pro661Arg
|
|
XM_017021586.1:c.1658C>G
|
XP_016877075.1:p.Pro553Arg
|
|
XM_017021587.1:c.1658C>G
|
XP_016877076.1:p.Pro553Arg
|
|
XM_017021588.1:c.1658C>G
|
XP_016877077.1:p.Pro553Arg
|
|
NM_001164749.2:c.1964C>G
MANE Select
|
NP_001158221.1:p.Pro655Arg
|
|
NM_001165893.2:c.1874C>G
|
NP_001159365.1:p.Pro625Arg
|
|
NM_022123.3:c.1868C>G
|
NP_071406.1:p.Pro623Arg
|
|
NM_173159.3:c.1925C>G
|
NP_775182.1:p.Pro642Arg
|
|
NM_001394988.1:c.1919C>G
|
NP_001381917.1:p.Pro640Arg
|
|
NM_001394989.1:c.1865C>G
|
NP_001381918.1:p.Pro622Arg
|
|