ENST00000684241.1:n.1947G>C
|
|
|
ENST00000262186.10:c.1114G>C
MANE Select
|
ENSP00000262186.5:p.Glu372Gln
|
|
ENST00000262186.9:c.1114G>C
|
ENSP00000262186.5:p.Glu372Gln
|
|
ENST00000430723.4:c.766G>C
|
ENSP00000387657.4:p.Glu256Gln
|
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ENST00000532957.5:n.1337G>C
|
|
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NM_000238.3:c.1114G>C , LRG_288t1:c.1114G>C
|
NP_000229.1:p.Glu372Gln
|
|
NM_172056.2:c.1114G>C , LRG_288t2:c.1114G>C
|
NP_742053.1:p.Glu372Gln
|
|
XM_011516185.1:c.814G>C
|
XP_011514487.1:p.Glu272Gln
|
|
XM_011516186.1:c.1114G>C
|
XP_011514488.1:p.Glu372Gln
|
|
XM_011516185.2:c.814G>C
|
XP_011514487.1:p.Glu272Gln
|
|
XM_011516186.3:c.1114G>C
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XP_011514488.1:p.Glu372Gln
|
|
XM_017012195.1:c.964G>C
|
XP_016867684.1:p.Glu322Gln
|
|
XM_017012196.1:c.937G>C
|
XP_016867685.1:p.Glu313Gln
|
|
NM_000238.4:c.1114G>C
MANE Select
|
NP_000229.1:p.Glu372Gln
|
|