ENST00000344537.10:c.286G>C
MANE Select
|
ENSP00000341680.6:p.Glu96Gln
|
|
ENST00000338950.9:c.286G>C
|
ENSP00000344718.5:p.Glu96Gln
|
|
ENST00000344537.9:c.286G>C
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ENSP00000341680.5:p.Glu96Gln
|
|
ENST00000355917.7:c.235G>C
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ENSP00000348183.4:p.Glu79Gln
|
|
ENST00000506844.1:c.*284G>C
|
ENSP00000424202.1:n.*284G>C
|
|
ENST00000510395.5:c.*196G>C
|
ENSP00000424685.1:n.*196G>C
|
|
ENST00000511762.2:c.181G>C
|
ENSP00000427473.2:p.Glu61Gln
|
|
ENST00000513680.5:c.*284G>C
|
ENSP00000424357.1:n.*284G>C
|
|
ENST00000515875.5:c.235G>C
|
ENSP00000425495.1:p.Glu79Gln
|
|
ENST00000622898.4:c.181G>C
|
ENSP00000481997.1:p.Glu61Gln
|
|
NM_001271667.1:c.43G>C
|
NP_001258596.1:p.Glu15Gln
|
|
NM_001271668.1:c.235G>C
|
NP_001258597.1:p.Glu79Gln
|
|
NM_001271669.1:c.181G>C
|
NP_001258598.1:p.Glu61Gln
|
|
NM_032122.4:c.286G>C , LRG_588t1:c.286G>C
|
NP_115498.2:p.Glu96Gln
|
|
NM_183040.2:c.286G>C , LRG_588t2:c.286G>C
|
NP_898861.1:p.Glu96Gln
|
|
NR_036448.1:n.614G>C
|
|
|
XM_005249447.3:c.247G>C
|
XP_005249504.1:p.Glu83Gln
|
|
XM_011514936.1:c.196G>C
|
XP_011513238.1:p.Glu66Gln
|
|
XM_005249447.4:c.247G>C
|
XP_005249504.1:p.Glu83Gln
|
|
XM_011514936.3:c.196G>C
|
XP_011513238.1:p.Glu66Gln
|
|
NM_032122.5:c.286G>C
MANE Select
|
NP_115498.2:p.Glu96Gln
|
|
NR_036448.2:n.584G>C
|
|
|
NM_001271667.2:c.43G>C
|
NP_001258596.1:p.Glu15Gln
|
|
NM_001271668.2:c.235G>C
|
NP_001258597.1:p.Glu79Gln
|
|
NM_001271669.2:c.181G>C
|
NP_001258598.1:p.Glu61Gln
|
|
NR_036448.3:n.584G>C
|
|
|