|
NM_001366722.1:c.1710A>T
MANE Select
|
NP_001353651.1:p.Gly570=
|
|
ENST00000359742.9:c.1710A>T
MANE Select
|
ENSP00000352780.4:p.Gly570=
|
|
NM_001178074.1:c.1554A>T
|
NP_001171545.1:p.Gly518=
|
|
NM_001178074.2:c.1554A>T
|
NP_001171545.1:p.Gly518=
|
|
NM_001366723.1:c.1629A>T
|
NP_001353652.1:p.Gly543=
|
|
NM_001366724.1:c.1632A>T
|
NP_001353653.1:p.Gly544=
|
|
NM_001379345.1:c.1788A>T
|
NP_001366274.1:p.Gly596=
|
|
NM_001379346.1:c.1710A>T
|
NP_001366275.1:p.Gly570=
|
|
NM_001379347.1:c.1632A>T
|
NP_001366276.1:p.Gly544=
|
|
NM_001379348.1:c.1629A>T
|
NP_001366277.1:p.Gly543=
|
|
NM_001379349.1:c.1557A>T
|
NP_001366278.1:p.Gly519=
|
|
NM_001379351.1:c.1554A>T
|
NP_001366280.1:p.Gly518=
|
|
NM_021150.3:c.1554A>T
|
NP_066973.2:p.Gly518=
|
|
NM_021150.4:c.1554A>T
|
NP_066973.2:p.Gly518=
|
|
ENST00000359742.8:c.1710A>T
|
ENSP00000352780.4:p.Gly570=
|
|
ENST00000398016.7:c.1554A>T
|
ENSP00000381098.3:p.Gly518=
|
|
ENST00000536215.5:c.1230A>T
|
ENSP00000446011.1:p.Gly410=
|
|
ENST00000538164.5:c.1154A>T
|
|
|
ENST00000538211.5:c.1554A>T
|
ENSP00000446047.1:p.Gly518=
|
|
ENST00000540433.5:c.1386A>T
|
ENSP00000446024.1:p.Gly462=
|
|
ENST00000540854.5:c.337+83013A>T
|
ENSP00000443006.1:n.337+83013A>T
|
|
ENST00000696989.1:c.1779A>T
|
ENSP00000513025.1:p.Gly593=
|
|
XM_005268754.3:c.1713A>T
|
XP_005268811.1:p.Gly571=
|
|
XM_005268754.4:c.1713A>T
|
XP_005268811.1:p.Gly571=
|
|
XM_005268757.3:c.1632A>T
|
XP_005268814.1:p.Gly544=
|
|
XM_005268757.4:c.1632A>T
|
XP_005268814.1:p.Gly544=
|
|
XM_011538089.1:c.1935A>T
|
XP_011536391.1:p.Gly645=
|
|
XM_011538090.1:c.1935A>T
|
XP_011536392.1:p.Gly645=
|
|
XM_011538091.1:c.1779A>T
|
XP_011536393.1:p.Gly593=
|
|
XM_011538092.1:c.1779A>T
|
XP_011536394.1:p.Gly593=
|
|
XM_011538093.1:c.1710A>T
|
XP_011536395.1:p.Gly570=
|
|
XM_011538094.1:c.1542A>T
|
XP_011536396.1:p.Gly514=
|
|
XM_017019098.1:c.1935A>T
|
XP_016874587.1:p.Gly645=
|
|
XM_017019099.1:c.1788A>T
|
XP_016874588.1:p.Gly596=
|
|
XM_017019100.1:c.1779A>T
|
XP_016874589.1:p.Gly593=
|
