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ENST00000375687.10:c.3257A>C
MANE Select
|
ENSP00000364839.4:p.Glu1086Ala
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|
|
ENST00000646985.1:c.3074A>C
|
ENSP00000495053.1:p.Glu1025Ala
|
|
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ENST00000647223.1:n.5610A>C
|
|
|
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ENST00000651418.1:c.1869+1388A>C
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ENSP00000499150.1:n.1869+1388A>C
|
|
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ENST00000306058.9:c.3242A>C
|
ENSP00000305119.5:p.Glu1081Ala
|
|
|
ENST00000375687.8:c.3257A>C
|
ENSP00000364839.4:p.Glu1086Ala
|
|
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ENST00000613218.4:c.3257A>C
|
ENSP00000480487.1:p.Glu1086Ala
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|
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ENST00000620121.4:c.3257A>C
|
ENSP00000481978.1:p.Glu1086Ala
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|
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NM_015338.5:c.3257A>C , LRG_630t1:c.3257A>C
|
NP_056153.2:p.Glu1086Ala
|
|
|
XM_006723727.2:c.3254A>C
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XP_006723790.1:p.Glu1085Ala
|
|
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XM_006723728.2:c.3227A>C
|
XP_006723791.1:p.Glu1076Ala
|
|
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XM_006723730.2:c.3173A>C
|
XP_006723793.1:p.Glu1058Ala
|
|
|
XM_006723732.2:c.3074A>C
|
XP_006723795.1:p.Glu1025Ala
|
|
|
XM_006723733.1:c.2573A>C
|
XP_006723796.1:p.Glu858Ala
|
|
|
XM_011528647.1:c.3521A>C
|
XP_011526949.1:p.Glu1174Ala
|
|
|
XM_011528648.1:c.3518A>C
|
XP_011526950.1:p.Glu1173Ala
|
|
|
XM_011528649.1:c.3437A>C
|
XP_011526951.1:p.Glu1146Ala
|
|
|
XM_011528650.1:c.3368A>C
|
XP_011526952.1:p.Glu1123Ala
|
|
|
XM_011528651.1:c.3236A>C
|
XP_011526953.1:p.Glu1079Ala
|
|
|
XM_011528652.1:c.3173A>C
|
XP_011526954.1:p.Glu1058Ala
|
|
|
NM_001363734.1:c.3074A>C
|
NP_001350663.1:p.Glu1025Ala
|
|
|
XM_006723727.3:c.3254A>C
|
XP_006723790.1:p.Glu1085Ala
|
|
|
XM_006723728.3:c.3227A>C
|
XP_006723791.1:p.Glu1076Ala
|
|
|
XM_006723730.4:c.3173A>C
|
XP_006723793.1:p.Glu1058Ala
|
|
|
XM_011528648.3:c.3518A>C
|
XP_011526950.1:p.Glu1173Ala
|
|
|
XM_011528652.2:c.3173A>C
|
XP_011526954.1:p.Glu1058Ala
|
|
|
XM_017027704.1:c.3173A>C
|
XP_016883193.1:p.Glu1058Ala
|
|
|
XM_017027705.1:c.3173A>C
|
XP_016883194.1:p.Glu1058Ala
|
|
|
XM_017027706.1:c.3104A>C
|
XP_016883195.1:p.Glu1035Ala
|
|
|
NM_015338.6:c.3257A>C
MANE Select
|
NP_056153.2:p.Glu1086Ala
|
|
