ENST00000375687.10:c.3984G>A
MANE Select
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ENSP00000364839.4:p.Glu1328=
|
|
ENST00000646985.1:c.3801G>A
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ENSP00000495053.1:p.Glu1267=
|
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ENST00000647223.1:n.6337G>A
|
|
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ENST00000651418.1:c.1870-1734G>A
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ENSP00000499150.1:n.1870-1734G>A
|
|
ENST00000306058.9:c.3969G>A
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ENSP00000305119.5:p.Glu1323=
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|
ENST00000375687.8:c.3984G>A
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ENSP00000364839.4:p.Glu1328=
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|
ENST00000613218.4:c.3984G>A
|
ENSP00000480487.1:p.Glu1328=
|
|
ENST00000620121.4:c.3984G>A
|
ENSP00000481978.1:p.Glu1328=
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NM_015338.5:c.3984G>A , LRG_630t1:c.3984G>A
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NP_056153.2:p.Glu1328=
|
|
XM_006723727.2:c.3981G>A
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XP_006723790.1:p.Glu1327=
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XM_006723728.2:c.3954G>A
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XP_006723791.1:p.Glu1318=
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XM_006723730.2:c.3900G>A
|
XP_006723793.1:p.Glu1300=
|
|
XM_006723732.2:c.3801G>A
|
XP_006723795.1:p.Glu1267=
|
|
XM_006723733.1:c.3300G>A
|
XP_006723796.1:p.Glu1100=
|
|
XM_011528647.1:c.4248G>A
|
XP_011526949.1:p.Glu1416=
|
|
XM_011528648.1:c.4245G>A
|
XP_011526950.1:p.Glu1415=
|
|
XM_011528649.1:c.4164G>A
|
XP_011526951.1:p.Glu1388=
|
|
XM_011528650.1:c.4095G>A
|
XP_011526952.1:p.Glu1365=
|
|
XM_011528651.1:c.3963G>A
|
XP_011526953.1:p.Glu1321=
|
|
XM_011528652.1:c.3900G>A
|
XP_011526954.1:p.Glu1300=
|
|
NM_001363734.1:c.3801G>A
|
NP_001350663.1:p.Glu1267=
|
|
XM_006723727.3:c.3981G>A
|
XP_006723790.1:p.Glu1327=
|
|
XM_006723728.3:c.3954G>A
|
XP_006723791.1:p.Glu1318=
|
|
XM_006723730.4:c.3900G>A
|
XP_006723793.1:p.Glu1300=
|
|
XM_011528648.3:c.4245G>A
|
XP_011526950.1:p.Glu1415=
|
|
XM_011528652.2:c.3900G>A
|
XP_011526954.1:p.Glu1300=
|
|
XM_017027704.1:c.3900G>A
|
XP_016883193.1:p.Glu1300=
|
|
XM_017027705.1:c.3900G>A
|
XP_016883194.1:p.Glu1300=
|
|
XM_017027706.1:c.3831G>A
|
XP_016883195.1:p.Glu1277=
|
|
NM_015338.6:c.3984G>A
MANE Select
|
NP_056153.2:p.Glu1328=
|
|