ENST00000461280.2:n.607G>C
|
|
|
ENST00000684116.1:n.202G>C
|
|
|
ENST00000684241.1:n.2142G>C
|
|
|
ENST00000262186.10:c.1309G>C
MANE Select
|
ENSP00000262186.5:p.Glu437Gln
|
|
ENST00000330883.9:c.289G>C
|
ENSP00000328531.4:p.Glu97Gln
|
|
ENST00000262186.9:c.1309G>C
|
ENSP00000262186.5:p.Glu437Gln
|
|
ENST00000330883.8:c.289G>C
|
ENSP00000328531.4:p.Glu97Gln
|
|
ENST00000430723.4:c.961G>C
|
ENSP00000387657.4:p.Glu321Gln
|
|
ENST00000461280.1:n.596G>C
|
|
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ENST00000473610.5:n.614G>C
|
|
|
ENST00000532957.5:n.1532G>C
|
|
|
NM_000238.3:c.1309G>C , LRG_288t1:c.1309G>C
|
NP_000229.1:p.Glu437Gln
|
|
NM_001204798.1:c.289G>C
|
NP_001191727.1:p.Glu97Gln
|
|
NM_172056.2:c.1309G>C , LRG_288t2:c.1309G>C
|
NP_742053.1:p.Glu437Gln
|
|
NM_172057.2:c.289G>C , LRG_288t3:c.289G>C
|
NP_742054.1:p.Glu97Gln
|
|
XM_011516185.1:c.1009G>C
|
XP_011514487.1:p.Glu337Gln
|
|
XM_011516186.1:c.1309G>C
|
XP_011514488.1:p.Glu437Gln
|
|
XM_011516185.2:c.1009G>C
|
XP_011514487.1:p.Glu337Gln
|
|
XM_011516186.3:c.1309G>C
|
XP_011514488.1:p.Glu437Gln
|
|
XM_017012195.1:c.1159G>C
|
XP_016867684.1:p.Glu387Gln
|
|
XM_017012196.1:c.1132G>C
|
XP_016867685.1:p.Glu378Gln
|
|
NM_000238.4:c.1309G>C
MANE Select
|
NP_000229.1:p.Glu437Gln
|
|
NM_001204798.2:c.289G>C
|
NP_001191727.1:p.Glu97Gln
|
|
NM_172057.3:c.289G>C
|
NP_742054.1:p.Glu97Gln
|
|