ENST00000356141.9:c.1783A>T
MANE Select
|
ENSP00000348460.4:p.Ser595Cys
|
|
ENST00000551634.6:c.1792A>T
|
ENSP00000448373.2:p.Ser598Cys
|
|
ENST00000680362.1:c.1683A>T
|
|
|
ENST00000681323.1:c.793+2509A>T
|
|
|
ENST00000346562.6:c.1687A>T
|
ENSP00000319610.5:p.Ser563Cys
|
|
ENST00000356141.8:c.1783A>T
|
ENSP00000348460.4:p.Ser595Cys
|
|
ENST00000357798.9:c.1744A>T
|
ENSP00000350446.5:p.Ser582Cys
|
|
ENST00000548645.5:c.1693A>T
|
ENSP00000448916.1:p.Ser565Cys
|
|
ENST00000551492.5:c.1798A>T
|
ENSP00000450392.1:p.Ser600Cys
|
|
ENST00000551634.5:c.1705A>T
|
ENSP00000448373.1:p.Ser569Cys
|
|
NM_001164749.1:c.1783A>T
|
NP_001158221.1:p.Ser595Cys
|
|
NM_001165893.1:c.1693A>T
|
NP_001159365.1:p.Ser565Cys
|
|
NM_022123.2:c.1687A>T
|
NP_071406.1:p.Ser563Cys
|
|
NM_173159.2:c.1744A>T
|
NP_775182.1:p.Ser582Cys
|
|
XM_005267991.2:c.1804A>T
|
XP_005268048.1:p.Ser602Cys
|
|
XM_005267992.2:c.1798A>T
|
XP_005268049.1:p.Ser600Cys
|
|
XM_005267993.2:c.1744A>T
|
XP_005268050.1:p.Ser582Cys
|
|
XM_011537067.1:c.1834A>T
|
XP_011535369.1:p.Ser612Cys
|
|
XM_011537068.1:c.1825A>T
|
XP_011535370.1:p.Ser609Cys
|
|
XM_011537069.1:c.1795A>T
|
XP_011535371.1:p.Ser599Cys
|
|
XM_011537070.1:c.1738A>T
|
XP_011535372.1:p.Ser580Cys
|
|
XM_011537071.1:c.1705A>T
|
XP_011535373.1:p.Ser569Cys
|
|
XM_011537072.1:c.1684A>T
|
XP_011535374.1:p.Ser562Cys
|
|
XM_011537073.1:c.1477A>T
|
XP_011535375.1:p.Ser493Cys
|
|
XM_011537074.1:c.1477A>T
|
XP_011535376.1:p.Ser493Cys
|
|
XM_005267991.3:c.1891A>T
|
XP_005268048.2:p.Ser631Cys
|
|
XM_005267992.3:c.1885A>T
|
XP_005268049.2:p.Ser629Cys
|
|
XM_011537067.2:c.1834A>T
|
XP_011535369.1:p.Ser612Cys
|
|
XM_011537069.2:c.1882A>T
|
XP_011535371.2:p.Ser628Cys
|
|
XM_011537070.2:c.1738A>T
|
XP_011535372.1:p.Ser580Cys
|
|
XM_011537071.2:c.1792A>T
|
XP_011535373.2:p.Ser598Cys
|
|
XM_011537072.2:c.1684A>T
|
XP_011535374.1:p.Ser562Cys
|
|
XM_017021582.1:c.1942A>T
|
XP_016877071.1:p.Ser648Cys
|
|
XM_017021583.1:c.1933A>T
|
XP_016877072.1:p.Ser645Cys
|
|
XM_017021584.1:c.1852A>T
|
XP_016877073.1:p.Ser618Cys
|
|
XM_017021585.1:c.1801A>T
|
XP_016877074.1:p.Ser601Cys
|
|
XM_017021586.1:c.1477A>T
|
XP_016877075.1:p.Ser493Cys
|
|
XM_017021587.1:c.1477A>T
|
XP_016877076.1:p.Ser493Cys
|
|
XM_017021588.1:c.1477A>T
|
XP_016877077.1:p.Ser493Cys
|
|
NM_001164749.2:c.1783A>T
MANE Select
|
NP_001158221.1:p.Ser595Cys
|
|
NM_001165893.2:c.1693A>T
|
NP_001159365.1:p.Ser565Cys
|
|
NM_022123.3:c.1687A>T
|
NP_071406.1:p.Ser563Cys
|
|
NM_173159.3:c.1744A>T
|
NP_775182.1:p.Ser582Cys
|
|
NM_001394988.1:c.1738A>T
|
NP_001381917.1:p.Ser580Cys
|
|
NM_001394989.1:c.1684A>T
|
NP_001381918.1:p.Ser562Cys
|
|