|
NM_144997.7:c.698G>C
MANE Select
|
NP_659434.2:p.Arg233Thr
|
|
ENST00000285071.9:c.698G>C
MANE Select
|
ENSP00000285071.4:p.Arg233Thr
|
|
NM_001353229.1:c.752G>C
|
NP_001340158.1:p.Arg251Thr
|
|
NM_001353229.2:c.752G>C
|
NP_001340158.1:p.Arg251Thr
|
|
NM_001353230.1:c.698G>C
|
NP_001340159.1:p.Arg233Thr
|
|
NM_001353230.2:c.698G>C
|
NP_001340159.1:p.Arg233Thr
|
|
NM_001353231.1:c.698G>C
|
NP_001340160.1:p.Arg233Thr
|
|
NM_001353231.2:c.698G>C
|
NP_001340160.1:p.Arg233Thr
|
|
NM_144606.5:c.698G>C
|
NP_653207.1:p.Arg233Thr
|
|
NM_144606.6:c.698G>C
|
NP_653207.1:p.Arg233Thr
|
|
NM_144606.7:c.698G>C
|
NP_653207.1:p.Arg233Thr
|
|
NM_144997.5:c.698G>C , LRG_325t1:c.698G>C
|
NP_659434.2:p.Arg233Thr
|
|
NM_144997.6:c.698G>C
|
NP_659434.2:p.Arg233Thr
|
|
ENST00000285071.8:c.698G>C
|
ENSP00000285071.4:p.Arg233Thr
|
|
ENST00000389169.9:c.698G>C
|
ENSP00000373821.5:p.Arg233Thr
|
|
ENST00000427497.3:c.149-3528G>C
|
ENSP00000394249.3:n.149-3528G>C
|
|
ENST00000466317.1:n.541G>C
|
|
|
ENST00000480316.1:n.664G>C
|
|
|
XM_011523714.1:c.752G>C
|
XP_011522016.1:p.Arg251Thr
|
|
XM_011523714.3:c.752G>C
|
XP_011522016.1:p.Arg251Thr
|
|
XM_011523715.1:c.752G>C
|
XP_011522017.1:p.Arg251Thr
|
|
XM_011523716.1:c.752G>C
|
XP_011522018.1:p.Arg251Thr
|
|
XM_011523717.1:c.752G>C
|
XP_011522019.1:p.Arg251Thr
|
|
XM_011523718.1:c.752G>C
|
XP_011522020.1:p.Arg251Thr
|
|
XM_011523718.3:c.752G>C
|
XP_011522020.1:p.Arg251Thr
|
|
XM_011523719.1:c.752G>C
|
XP_011522021.1:p.Arg251Thr
|
|
XM_011523719.3:c.752G>C
|
XP_011522021.1:p.Arg251Thr
|
|
XM_011523720.1:c.476G>C
|
XP_011522022.1:p.Arg159Thr
|
|
XM_011523721.1:c.752G>C
|
XP_011522023.1:p.Arg251Thr
|
|
XM_011523721.3:c.752G>C
|
XP_011522023.1:p.Arg251Thr
|
|
XM_017024305.2:c.752G>C
|
XP_016879794.1:p.Arg251Thr
|
|
XM_017024308.1:c.698G>C
|
XP_016879797.1:p.Arg233Thr
|
|
XM_017024309.2:c.476G>C
|
XP_016879798.1:p.Arg159Thr
|
|
XM_024450635.1:c.752G>C
|
XP_024306403.1:p.Arg251Thr
|
|
XR_001752445.2:n.1256G>C
|
|
|
XR_934007.1:n.2092G>C
|
|
