ENST00000356141.9:c.1981G>A
MANE Select
|
ENSP00000348460.4:p.Asp661Asn
|
|
ENST00000551634.6:c.1990G>A
|
ENSP00000448373.2:p.Asp664Asn
|
|
ENST00000680362.1:c.1881G>A
|
|
|
ENST00000681323.1:c.793+2707G>A
|
|
|
ENST00000346562.6:c.1885G>A
|
ENSP00000319610.5:p.Asp629Asn
|
|
ENST00000356141.8:c.1981G>A
|
ENSP00000348460.4:p.Asp661Asn
|
|
ENST00000357798.9:c.1942G>A
|
ENSP00000350446.5:p.Asp648Asn
|
|
ENST00000548645.5:c.1891G>A
|
ENSP00000448916.1:p.Asp631Asn
|
|
ENST00000551492.5:c.1996G>A
|
ENSP00000450392.1:p.Asp666Asn
|
|
ENST00000551634.5:c.1903G>A
|
ENSP00000448373.1:p.Asp635Asn
|
|
NM_001164749.1:c.1981G>A
|
NP_001158221.1:p.Asp661Asn
|
|
NM_001165893.1:c.1891G>A
|
NP_001159365.1:p.Asp631Asn
|
|
NM_022123.2:c.1885G>A
|
NP_071406.1:p.Asp629Asn
|
|
NM_173159.2:c.1942G>A
|
NP_775182.1:p.Asp648Asn
|
|
XM_005267991.2:c.2002G>A
|
XP_005268048.1:p.Asp668Asn
|
|
XM_005267992.2:c.1996G>A
|
XP_005268049.1:p.Asp666Asn
|
|
XM_005267993.2:c.1942G>A
|
XP_005268050.1:p.Asp648Asn
|
|
XM_011537067.1:c.2032G>A
|
XP_011535369.1:p.Asp678Asn
|
|
XM_011537068.1:c.2023G>A
|
XP_011535370.1:p.Asp675Asn
|
|
XM_011537069.1:c.1993G>A
|
XP_011535371.1:p.Asp665Asn
|
|
XM_011537070.1:c.1936G>A
|
XP_011535372.1:p.Asp646Asn
|
|
XM_011537071.1:c.1903G>A
|
XP_011535373.1:p.Asp635Asn
|
|
XM_011537072.1:c.1882G>A
|
XP_011535374.1:p.Asp628Asn
|
|
XM_011537073.1:c.1675G>A
|
XP_011535375.1:p.Asp559Asn
|
|
XM_011537074.1:c.1675G>A
|
XP_011535376.1:p.Asp559Asn
|
|
XM_005267991.3:c.2089G>A
|
XP_005268048.2:p.Asp697Asn
|
|
XM_005267992.3:c.2083G>A
|
XP_005268049.2:p.Asp695Asn
|
|
XM_011537067.2:c.2032G>A
|
XP_011535369.1:p.Asp678Asn
|
|
XM_011537069.2:c.2080G>A
|
XP_011535371.2:p.Asp694Asn
|
|
XM_011537070.2:c.1936G>A
|
XP_011535372.1:p.Asp646Asn
|
|
XM_011537071.2:c.1990G>A
|
XP_011535373.2:p.Asp664Asn
|
|
XM_011537072.2:c.1882G>A
|
XP_011535374.1:p.Asp628Asn
|
|
XM_017021582.1:c.2140G>A
|
XP_016877071.1:p.Asp714Asn
|
|
XM_017021583.1:c.2131G>A
|
XP_016877072.1:p.Asp711Asn
|
|
XM_017021584.1:c.2050G>A
|
XP_016877073.1:p.Asp684Asn
|
|
XM_017021585.1:c.1999G>A
|
XP_016877074.1:p.Asp667Asn
|
|
XM_017021586.1:c.1675G>A
|
XP_016877075.1:p.Asp559Asn
|
|
XM_017021587.1:c.1675G>A
|
XP_016877076.1:p.Asp559Asn
|
|
XM_017021588.1:c.1675G>A
|
XP_016877077.1:p.Asp559Asn
|
|
NM_001164749.2:c.1981G>A
MANE Select
|
NP_001158221.1:p.Asp661Asn
|
|
NM_001165893.2:c.1891G>A
|
NP_001159365.1:p.Asp631Asn
|
|
NM_022123.3:c.1885G>A
|
NP_071406.1:p.Asp629Asn
|
|
NM_173159.3:c.1942G>A
|
NP_775182.1:p.Asp648Asn
|
|
NM_001394988.1:c.1936G>A
|
NP_001381917.1:p.Asp646Asn
|
|
NM_001394989.1:c.1882G>A
|
NP_001381918.1:p.Asp628Asn
|
|