ENST00000356141.9:c.2092G>C
MANE Select
|
ENSP00000348460.4:p.Gly698Arg
|
|
ENST00000551634.6:c.2101G>C
|
ENSP00000448373.2:p.Gly701Arg
|
|
ENST00000680362.1:c.1992G>C
|
|
|
ENST00000681323.1:c.793+2818G>C
|
|
|
ENST00000346562.6:c.1996G>C
|
ENSP00000319610.5:p.Gly666Arg
|
|
ENST00000356141.8:c.2092G>C
|
ENSP00000348460.4:p.Gly698Arg
|
|
ENST00000357798.9:c.2053G>C
|
ENSP00000350446.5:p.Gly685Arg
|
|
ENST00000548645.5:c.2002G>C
|
ENSP00000448916.1:p.Gly668Arg
|
|
ENST00000551492.5:c.2107G>C
|
ENSP00000450392.1:p.Gly703Arg
|
|
ENST00000551634.5:c.2014G>C
|
ENSP00000448373.1:p.Gly672Arg
|
|
NM_001164749.1:c.2092G>C
|
NP_001158221.1:p.Gly698Arg
|
|
NM_001165893.1:c.2002G>C
|
NP_001159365.1:p.Gly668Arg
|
|
NM_022123.2:c.1996G>C
|
NP_071406.1:p.Gly666Arg
|
|
NM_173159.2:c.2053G>C
|
NP_775182.1:p.Gly685Arg
|
|
XM_005267991.2:c.2113G>C
|
XP_005268048.1:p.Gly705Arg
|
|
XM_005267992.2:c.2107G>C
|
XP_005268049.1:p.Gly703Arg
|
|
XM_005267993.2:c.2053G>C
|
XP_005268050.1:p.Gly685Arg
|
|
XM_011537067.1:c.2143G>C
|
XP_011535369.1:p.Gly715Arg
|
|
XM_011537068.1:c.2134G>C
|
XP_011535370.1:p.Gly712Arg
|
|
XM_011537069.1:c.2104G>C
|
XP_011535371.1:p.Gly702Arg
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|
XM_011537070.1:c.2047G>C
|
XP_011535372.1:p.Gly683Arg
|
|
XM_011537071.1:c.2014G>C
|
XP_011535373.1:p.Gly672Arg
|
|
XM_011537072.1:c.1993G>C
|
XP_011535374.1:p.Gly665Arg
|
|
XM_011537073.1:c.1786G>C
|
XP_011535375.1:p.Gly596Arg
|
|
XM_011537074.1:c.1786G>C
|
XP_011535376.1:p.Gly596Arg
|
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XM_005267991.3:c.2200G>C
|
XP_005268048.2:p.Gly734Arg
|
|
XM_005267992.3:c.2194G>C
|
XP_005268049.2:p.Gly732Arg
|
|
XM_011537067.2:c.2143G>C
|
XP_011535369.1:p.Gly715Arg
|
|
XM_011537069.2:c.2191G>C
|
XP_011535371.2:p.Gly731Arg
|
|
XM_011537070.2:c.2047G>C
|
XP_011535372.1:p.Gly683Arg
|
|
XM_011537071.2:c.2101G>C
|
XP_011535373.2:p.Gly701Arg
|
|
XM_011537072.2:c.1993G>C
|
XP_011535374.1:p.Gly665Arg
|
|
XM_017021582.1:c.2251G>C
|
XP_016877071.1:p.Gly751Arg
|
|
XM_017021583.1:c.2242G>C
|
XP_016877072.1:p.Gly748Arg
|
|
XM_017021584.1:c.2161G>C
|
XP_016877073.1:p.Gly721Arg
|
|
XM_017021585.1:c.2110G>C
|
XP_016877074.1:p.Gly704Arg
|
|
XM_017021586.1:c.1786G>C
|
XP_016877075.1:p.Gly596Arg
|
|
XM_017021587.1:c.1786G>C
|
XP_016877076.1:p.Gly596Arg
|
|
XM_017021588.1:c.1786G>C
|
XP_016877077.1:p.Gly596Arg
|
|
NM_001164749.2:c.2092G>C
MANE Select
|
NP_001158221.1:p.Gly698Arg
|
|
NM_001165893.2:c.2002G>C
|
NP_001159365.1:p.Gly668Arg
|
|
NM_022123.3:c.1996G>C
|
NP_071406.1:p.Gly666Arg
|
|
NM_173159.3:c.2053G>C
|
NP_775182.1:p.Gly685Arg
|
|
NM_001394988.1:c.2047G>C
|
NP_001381917.1:p.Gly683Arg
|
|
NM_001394989.1:c.1993G>C
|
NP_001381918.1:p.Gly665Arg
|
|