ENST00000262494.13:c.710A>T
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ENSP00000262494.7:p.Glu237Val
|
|
ENST00000262493.12:c.710A>T
MANE Select
|
ENSP00000262493.6:p.Glu237Val
|
|
ENST00000262494.12:c.710A>T
|
ENSP00000262494.7:p.Glu237Val
|
|
ENST00000562316.6:c.377A>T
|
ENSP00000457238.2:p.Glu126Val
|
|
ENST00000564727.2:c.14A>T
|
ENSP00000454971.2:p.Glu5Val
|
|
ENST00000568375.2:c.102A>T
|
|
|
ENST00000638185.1:n.925A>T
|
|
|
ENST00000638210.1:n.1010A>T
|
|
|
ENST00000638705.1:c.710A>T
|
ENSP00000491223.1:p.Glu237Val
|
|
ENST00000638836.1:n.620A>T
|
|
|
ENST00000639055.1:n.1431A>T
|
|
|
ENST00000639251.1:n.611A>T
|
|
|
ENST00000639268.1:c.345A>T
|
|
|
ENST00000639341.1:c.235A>T
|
|
|
ENST00000639770.1:c.748A>T
|
ENSP00000491999.1:n.748A>T
|
|
ENST00000640390.1:n.640A>T
|
|
|
ENST00000640469.1:c.74A>T
|
ENSP00000491875.1:p.Glu25Val
|
|
ENST00000640560.1:n.486A>T
|
|
|
ENST00000640893.1:c.*108A>T
|
ENSP00000492677.1:n.*108A>T
|
|
ENST00000262493.10:c.710A>T
|
ENSP00000262493.6:p.Glu237Val
|
|
ENST00000262494.11:c.710A>T
|
ENSP00000262494.7:p.Glu237Val
|
|
ENST00000568375.1:n.102A>T
|
|
|
NM_020988.2:c.710A>T
|
NP_066268.1:p.Glu237Val
|
|
NM_138736.2:c.710A>T
|
NP_620073.2:p.Glu237Val
|
|
XM_011523003.1:c.584A>T
|
XP_011521305.1:p.Glu195Val
|
|
XM_011523003.3:c.584A>T
|
XP_011521305.1:p.Glu195Val
|
|
NM_020988.3:c.710A>T
MANE Select
|
NP_066268.1:p.Glu237Val
|
|
NM_138736.3:c.710A>T
|
NP_620073.2:p.Glu237Val
|
|