|
NM_015404.4:c.2256G=
MANE Select
|
NP_056219.3:p.Gln752=
|
|
ENST00000362057.4:c.2256G=
MANE Select
|
ENSP00000354623.3:p.Gln752=
|
|
NM_001083885.2:c.1107G=
|
NP_001077354.2:p.Gln369=
|
|
NM_001083885.3:c.1107G=
|
NP_001077354.2:p.Gln369=
|
|
NM_001173425.1:c.2253G=
|
NP_001166896.1:p.Gln751=
|
|
NM_001173425.2:c.2253G=
|
NP_001166896.1:p.Gln751=
|
|
NM_001346890.1:c.1203G=
|
NP_001333819.1:p.Gln401=
|
|
NM_015404.3:c.2256G=
|
NP_056219.3:p.Gln752=
|
|
ENST00000265134.10:c.1107G=
|
ENSP00000265134.6:p.Gln369=
|
|
ENST00000362057.3:c.2256G=
|
ENSP00000354623.3:p.Gln752=
|
|
ENST00000374059.7:c.1203G=
|
ENSP00000363172.3:p.Gln401=
|
|
ENST00000674036.8:c.1229G=
|
|
|
ENST00000674048.1:n.2137G=
|
|
|
ENST00000699485.1:c.600G=
|
ENSP00000514396.1:p.Gln200=
|
|
XM_005251897.3:c.1593G=
|
XP_005251954.2:p.Gln531=
|
|
XM_011518484.1:c.2289G=
|
XP_011516786.1:p.Gln763=
|
|
XM_011518485.1:c.2289G=
|
XP_011516787.1:p.Gln763=
|
|
XM_011518486.1:c.2286G=
|
XP_011516788.1:p.Gln762=
|
|
XM_011518486.2:c.2286G=
|
XP_011516788.1:p.Gln762=
|
|
XM_011518487.1:c.2163G=
|
XP_011516789.1:p.Gln721=
|
|
XM_011518487.2:c.2163G=
|
XP_011516789.1:p.Gln721=
|
|
XM_011518488.1:c.2046G=
|
XP_011516790.1:p.Gln682=
|
|
XM_011518488.2:c.2046G=
|
XP_011516790.1:p.Gln682=
|
|
XM_011518495.1:c.966G=
|
XP_011516797.1:p.Gln322=
|
|
XR_929747.1:n.3193G=
|
|
|
XR_929747.2:n.2504G=
|
|
|
XR_929748.1:n.3091G=
|
|
|
XR_929748.2:n.2402G=
|
|
