ENST00000481478.2:c.5178C>A
|
ENSP00000418014.2:p.Thr1726=
|
|
ENST00000636633.2:n.2194-77C>A
|
|
|
ENST00000636999.2:n.553C>A
|
|
|
ENST00000288139.11:c.5178C>A
MANE Plus Clinical
|
ENSP00000288139.3:p.Thr1726=
|
|
ENST00000350061.11:c.5118C>A
MANE Select
|
ENSP00000288133.5:p.Thr1706=
|
|
ENST00000422281.7:c.5073C>A
|
ENSP00000409174.2:p.Thr1691=
|
|
ENST00000636448.1:c.1316-77C>A
|
|
|
ENST00000636570.1:c.5073C>A
|
ENSP00000490183.1:p.Thr1691=
|
|
ENST00000636629.1:n.474C>A
|
|
|
ENST00000636633.1:n.2194-77C>A
|
|
|
ENST00000636999.1:n.545C>A
|
|
|
ENST00000637424.1:c.5145C>A
|
ENSP00000489769.1:p.Thr1715=
|
|
ENST00000288139.8:c.5178C>A
|
ENSP00000288139.3:p.Thr1726=
|
|
ENST00000350061.9:c.5118C>A
|
ENSP00000288133.5:p.Thr1706=
|
|
ENST00000422281.6:c.5073C>A
|
ENSP00000409174.2:p.Thr1691=
|
|
ENST00000481478.1:c.4197C>A
|
ENSP00000418014.1:p.Thr1399=
|
|
NM_000720.3:c.5178C>A
|
NP_000711.1:p.Thr1726=
|
|
NM_001128839.2:c.5073C>A
|
NP_001122311.1:p.Thr1691=
|
|
NM_001128840.2:c.5118C>A
|
NP_001122312.1:p.Thr1706=
|
|
XM_005265448.2:c.5073C>A
|
XP_005265505.1:p.Thr1691=
|
|
XM_011534094.1:c.5373C>A
|
XP_011532396.1:p.Thr1791=
|
|
XM_011534095.1:c.5262C>A
|
XP_011532397.1:p.Thr1754=
|
|
XM_011534096.1:c.5184C>A
|
XP_011532398.1:p.Thr1728=
|
|
XM_011534097.1:c.4836C>A
|
XP_011532399.1:p.Thr1612=
|
|
XM_011534098.1:c.4836C>A
|
XP_011532400.1:p.Thr1612=
|
|
XM_011534099.1:c.4461C>A
|
XP_011532401.1:p.Thr1487=
|
|
XM_011534100.1:c.5268C>A
|
XP_011532402.1:p.Thr1756=
|
|
XM_005265448.3:c.5073C>A
|
XP_005265505.1:p.Thr1691=
|
|
XM_011534094.2:c.5373C>A
|
XP_011532396.1:p.Thr1791=
|
|
XM_011534096.2:c.5184C>A
|
XP_011532398.1:p.Thr1728=
|
|
XM_011534097.2:c.4836C>A
|
XP_011532399.1:p.Thr1612=
|
|
XM_011534099.2:c.4461C>A
|
XP_011532401.1:p.Thr1487=
|
|
XM_011534100.2:c.5268C>A
|
XP_011532402.1:p.Thr1756=
|
|
XM_017007137.1:c.5373C>A
|
XP_016862626.1:p.Thr1791=
|
|
XM_017007138.1:c.5370C>A
|
XP_016862627.1:p.Thr1790=
|
|
XM_017007139.1:c.5373C>A
|
XP_016862628.1:p.Thr1791=
|
|
XM_017007140.1:c.5313C>A
|
XP_016862629.1:p.Thr1771=
|
|
XM_017007141.1:c.5313C>A
|
XP_016862630.1:p.Thr1771=
|
|
XM_017007142.1:c.5289C>A
|
XP_016862631.1:p.Thr1763=
|
|
XM_017007143.1:c.5289C>A
|
XP_016862632.1:p.Thr1763=
|
|
XM_017007144.1:c.5289C>A
|
XP_016862633.1:p.Thr1763=
|
|
XM_017007145.1:c.5244C>A
|
XP_016862634.1:p.Thr1748=
|
|
NM_001128840.3:c.5118C>A
MANE Select
|
NP_001122312.1:p.Thr1706=
|
|
NM_000720.4:c.5178C>A
MANE Plus Clinical
|
NP_000711.1:p.Thr1726=
|
|
NM_001128839.3:c.5073C>A
|
NP_001122311.1:p.Thr1691=
|
|