ENST00000356141.9:c.1922A>C
MANE Select
|
ENSP00000348460.4:p.Asn641Thr
|
|
ENST00000551634.6:c.1931A>C
|
ENSP00000448373.2:p.Asn644Thr
|
|
ENST00000680362.1:c.1822A>C
|
|
|
ENST00000681323.1:c.793+2648A>C
|
|
|
ENST00000346562.6:c.1826A>C
|
ENSP00000319610.5:p.Asn609Thr
|
|
ENST00000356141.8:c.1922A>C
|
ENSP00000348460.4:p.Asn641Thr
|
|
ENST00000357798.9:c.1883A>C
|
ENSP00000350446.5:p.Asn628Thr
|
|
ENST00000548645.5:c.1832A>C
|
ENSP00000448916.1:p.Asn611Thr
|
|
ENST00000551492.5:c.1937A>C
|
ENSP00000450392.1:p.Asn646Thr
|
|
ENST00000551634.5:c.1844A>C
|
ENSP00000448373.1:p.Asn615Thr
|
|
NM_001164749.1:c.1922A>C
|
NP_001158221.1:p.Asn641Thr
|
|
NM_001165893.1:c.1832A>C
|
NP_001159365.1:p.Asn611Thr
|
|
NM_022123.2:c.1826A>C
|
NP_071406.1:p.Asn609Thr
|
|
NM_173159.2:c.1883A>C
|
NP_775182.1:p.Asn628Thr
|
|
XM_005267991.2:c.1943A>C
|
XP_005268048.1:p.Asn648Thr
|
|
XM_005267992.2:c.1937A>C
|
XP_005268049.1:p.Asn646Thr
|
|
XM_005267993.2:c.1883A>C
|
XP_005268050.1:p.Asn628Thr
|
|
XM_011537067.1:c.1973A>C
|
XP_011535369.1:p.Asn658Thr
|
|
XM_011537068.1:c.1964A>C
|
XP_011535370.1:p.Asn655Thr
|
|
XM_011537069.1:c.1934A>C
|
XP_011535371.1:p.Asn645Thr
|
|
XM_011537070.1:c.1877A>C
|
XP_011535372.1:p.Asn626Thr
|
|
XM_011537071.1:c.1844A>C
|
XP_011535373.1:p.Asn615Thr
|
|
XM_011537072.1:c.1823A>C
|
XP_011535374.1:p.Asn608Thr
|
|
XM_011537073.1:c.1616A>C
|
XP_011535375.1:p.Asn539Thr
|
|
XM_011537074.1:c.1616A>C
|
XP_011535376.1:p.Asn539Thr
|
|
XM_005267991.3:c.2030A>C
|
XP_005268048.2:p.Asn677Thr
|
|
XM_005267992.3:c.2024A>C
|
XP_005268049.2:p.Asn675Thr
|
|
XM_011537067.2:c.1973A>C
|
XP_011535369.1:p.Asn658Thr
|
|
XM_011537069.2:c.2021A>C
|
XP_011535371.2:p.Asn674Thr
|
|
XM_011537070.2:c.1877A>C
|
XP_011535372.1:p.Asn626Thr
|
|
XM_011537071.2:c.1931A>C
|
XP_011535373.2:p.Asn644Thr
|
|
XM_011537072.2:c.1823A>C
|
XP_011535374.1:p.Asn608Thr
|
|
XM_017021582.1:c.2081A>C
|
XP_016877071.1:p.Asn694Thr
|
|
XM_017021583.1:c.2072A>C
|
XP_016877072.1:p.Asn691Thr
|
|
XM_017021584.1:c.1991A>C
|
XP_016877073.1:p.Asn664Thr
|
|
XM_017021585.1:c.1940A>C
|
XP_016877074.1:p.Asn647Thr
|
|
XM_017021586.1:c.1616A>C
|
XP_016877075.1:p.Asn539Thr
|
|
XM_017021587.1:c.1616A>C
|
XP_016877076.1:p.Asn539Thr
|
|
XM_017021588.1:c.1616A>C
|
XP_016877077.1:p.Asn539Thr
|
|
NM_001164749.2:c.1922A>C
MANE Select
|
NP_001158221.1:p.Asn641Thr
|
|
NM_001165893.2:c.1832A>C
|
NP_001159365.1:p.Asn611Thr
|
|
NM_022123.3:c.1826A>C
|
NP_071406.1:p.Asn609Thr
|
|
NM_173159.3:c.1883A>C
|
NP_775182.1:p.Asn628Thr
|
|
NM_001394988.1:c.1877A>C
|
NP_001381917.1:p.Asn626Thr
|
|
NM_001394989.1:c.1823A>C
|
NP_001381918.1:p.Asn608Thr
|
|