ENST00000379565.9:c.1287A>T
MANE Select
|
ENSP00000368884.3:p.Gly429=
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|
ENST00000457145.6:c.1200A>T
|
ENSP00000407655.2:p.Gly400=
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|
ENST00000642835.1:c.1203A>T
|
ENSP00000494769.1:p.Gly401=
|
|
ENST00000643073.1:c.905A>T
|
ENSP00000495839.1:n.905A>T
|
|
ENST00000643085.1:c.1203A>T
|
ENSP00000496271.1:p.Gly401=
|
|
ENST00000643337.1:c.1203A>T
|
ENSP00000493487.1:p.Gly401=
|
|
ENST00000643402.1:c.1203A>T
|
ENSP00000493862.1:p.Gly401=
|
|
ENST00000644368.1:c.1203A>T
|
ENSP00000495776.1:p.Gly401=
|
|
ENST00000644893.1:c.1200A>T
|
ENSP00000495974.1:p.Gly400=
|
|
ENST00000645268.1:c.*508A>T
|
ENSP00000496226.1:n.*508A>T
|
|
ENST00000645270.1:c.1203A>T
|
ENSP00000494967.1:p.Gly401=
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|
ENST00000646610.1:c.1203A>T
|
ENSP00000495462.1:p.Gly401=
|
|
ENST00000647265.1:c.1203A>T
|
ENSP00000494220.1:p.Gly401=
|
|
ENST00000379565.7:c.1287A>T
|
ENSP00000368884.3:p.Gly429=
|
|
ENST00000479809.1:n.53A>T
|
|
|
NM_004586.2:c.1287A>T
|
NP_004577.1:p.Gly429=
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|
XM_005274573.2:c.1284A>T
|
XP_005274630.1:p.Gly428=
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|
XM_005274577.2:c.1197A>T
|
XP_005274634.1:p.Gly399=
|
|
XM_006724507.2:c.1200A>T
|
XP_006724570.1:p.Gly400=
|
|
XM_011545555.1:c.1305A>T
|
XP_011543857.1:p.Gly435=
|
|
XM_011545556.1:c.1302A>T
|
XP_011543858.1:p.Gly434=
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|
XM_011545557.1:c.1221A>T
|
XP_011543859.1:p.Gly407=
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|
XM_011545558.1:c.1221A>T
|
XP_011543860.1:p.Gly407=
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|
XM_011545559.1:c.1221A>T
|
XP_011543861.1:p.Gly407=
|
|
XM_011545560.1:c.1221A>T
|
XP_011543862.1:p.Gly407=
|
|
XM_011545561.1:c.1221A>T
|
XP_011543863.1:p.Gly407=
|
|
XM_011545562.1:c.1218A>T
|
XP_011543864.1:p.Gly406=
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|
XM_011545563.1:c.1203A>T
|
XP_011543865.1:p.Gly401=
|
|
XM_005274577.3:c.1197A>T
|
XP_005274634.1:p.Gly399=
|
|
XM_006724507.3:c.1200A>T
|
XP_006724570.1:p.Gly400=
|
|
XM_011545557.2:c.1221A>T
|
XP_011543859.1:p.Gly407=
|
|
XM_011545558.2:c.1221A>T
|
XP_011543860.1:p.Gly407=
|
|
XM_011545561.2:c.1221A>T
|
XP_011543863.1:p.Gly407=
|
|
XM_011545562.2:c.1218A>T
|
XP_011543864.1:p.Gly406=
|
|
XM_011545563.3:c.1203A>T
|
XP_011543865.1:p.Gly401=
|
|
XM_017029713.1:c.1203A>T
|
XP_016885202.1:p.Gly401=
|
|
XM_017029714.2:c.1203A>T
|
XP_016885203.1:p.Gly401=
|
|
XM_017029715.2:c.1203A>T
|
XP_016885204.1:p.Gly401=
|
|
XM_017029716.1:c.1203A>T
|
XP_016885205.1:p.Gly401=
|
|
XM_017029717.2:c.1203A>T
|
XP_016885206.1:p.Gly401=
|
|
XM_017029718.2:c.1200A>T
|
XP_016885207.1:p.Gly400=
|
|
XM_017029719.2:c.1200A>T
|
XP_016885208.1:p.Gly400=
|
|
NM_004586.3:c.1287A>T
MANE Select
|
NP_004577.1:p.Gly429=
|
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