ENST00000350721.9:c.4638G>T
MANE Select
|
ENSP00000343741.4:p.Gln1546His
|
|
ENST00000653868.1:n.4667G>T
|
|
|
ENST00000656590.1:c.3428G>T
|
|
|
ENST00000661310.1:c.4446G>T
|
ENSP00000499589.1:p.Gln1482His
|
|
ENST00000666943.1:n.102G>T
|
|
|
ENST00000350721.8:c.4638G>T
|
ENSP00000343741.4:p.Gln1546His
|
|
NM_001184.3:c.4638G>T
|
NP_001175.2:p.Gln1546His
|
|
XM_011512924.1:c.4644G>T
|
XP_011511226.1:p.Gln1548His
|
|
XM_011512925.1:c.4452G>T
|
XP_011511227.1:p.Gln1484His
|
|
XM_011512926.1:c.4644G>T
|
XP_011511228.1:p.Gln1548His
|
|
XM_011512927.1:c.4644G>T
|
XP_011511229.1:p.Gln1548His
|
|
XR_924147.1:n.4733G>T
|
|
|
XR_924148.1:n.4733G>T
|
|
|
XR_924149.1:n.4733G>T
|
|
|
NM_001354579.1:c.4446G>T
|
NP_001341508.1:p.Gln1482His
|
|
XR_001740179.2:n.4727G>T
|
|
|
XR_001740180.2:n.4733G>T
|
|
|
XR_001740181.2:n.4733G>T
|
|
|
XR_001740182.1:n.4733G>T
|
|
|
XR_002959543.1:n.4733G>T
|
|
|
XR_924148.2:n.4733G>T
|
|
|
NM_001184.4:c.4638G>T
MANE Select
|
NP_001175.2:p.Gln1546His
|
|
NM_001354579.2:c.4446G>T
|
NP_001341508.1:p.Gln1482His
|
|