ENST00000262367.10:c.5415C>G
MANE Select
|
ENSP00000262367.5:p.Thr1805=
|
|
ENST00000262367.9:c.5415C>G
|
ENSP00000262367.5:p.Thr1805=
|
|
ENST00000382070.7:c.5301C>G
|
ENSP00000371502.3:p.Thr1767=
|
|
NM_001079846.1:c.5301C>G
|
NP_001073315.1:p.Thr1767=
|
|
NM_004380.2:c.5415C>G
|
NP_004371.2:p.Thr1805=
|
|
XM_005255124.3:c.5370C>G
|
XP_005255181.1:p.Thr1790=
|
|
XM_005255125.3:c.4998C>G
|
XP_005255182.1:p.Thr1666=
|
|
XM_006720848.2:c.5154C>G
|
XP_006720911.1:p.Thr1718=
|
|
XM_011522380.1:c.5361C>G
|
XP_011520682.1:p.Thr1787=
|
|
XM_011522381.1:c.4662C>G
|
XP_011520683.1:p.Thr1554=
|
|
XM_005255124.4:c.5370C>G
|
XP_005255181.1:p.Thr1790=
|
|
XM_005255125.4:c.4998C>G
|
XP_005255182.1:p.Thr1666=
|
|
XM_006720848.3:c.5154C>G
|
XP_006720911.1:p.Thr1718=
|
|
XM_011522381.2:c.4662C>G
|
XP_011520683.1:p.Thr1554=
|
|
XM_017022944.1:c.5409C>G
|
XP_016878433.1:p.Thr1803=
|
|
NM_004380.3:c.5415C>G
MANE Select
|
NP_004371.2:p.Thr1805=
|
|