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ENST00000375687.10:c.3575A>C
MANE Select
|
ENSP00000364839.4:p.Glu1192Ala
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ENST00000646985.1:c.3392A>C
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ENSP00000495053.1:p.Glu1131Ala
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ENST00000647223.1:n.5928A>C
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ENST00000651418.1:c.1869+1706A>C
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ENSP00000499150.1:n.1869+1706A>C
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ENST00000306058.9:c.3560A>C
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ENSP00000305119.5:p.Glu1187Ala
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ENST00000375687.8:c.3575A>C
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ENSP00000364839.4:p.Glu1192Ala
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ENST00000613218.4:c.3575A>C
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ENSP00000480487.1:p.Glu1192Ala
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ENST00000620121.4:c.3575A>C
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ENSP00000481978.1:p.Glu1192Ala
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NM_015338.5:c.3575A>C , LRG_630t1:c.3575A>C
|
NP_056153.2:p.Glu1192Ala
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XM_006723727.2:c.3572A>C
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XP_006723790.1:p.Glu1191Ala
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XM_006723728.2:c.3545A>C
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XP_006723791.1:p.Glu1182Ala
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XM_006723730.2:c.3491A>C
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XP_006723793.1:p.Glu1164Ala
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XM_006723732.2:c.3392A>C
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XP_006723795.1:p.Glu1131Ala
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|
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XM_006723733.1:c.2891A>C
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XP_006723796.1:p.Glu964Ala
|
|
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XM_011528647.1:c.3839A>C
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XP_011526949.1:p.Glu1280Ala
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|
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XM_011528648.1:c.3836A>C
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XP_011526950.1:p.Glu1279Ala
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|
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XM_011528649.1:c.3755A>C
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XP_011526951.1:p.Glu1252Ala
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|
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XM_011528650.1:c.3686A>C
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XP_011526952.1:p.Glu1229Ala
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|
|
XM_011528651.1:c.3554A>C
|
XP_011526953.1:p.Glu1185Ala
|
|
|
XM_011528652.1:c.3491A>C
|
XP_011526954.1:p.Glu1164Ala
|
|
|
NM_001363734.1:c.3392A>C
|
NP_001350663.1:p.Glu1131Ala
|
|
|
XM_006723727.3:c.3572A>C
|
XP_006723790.1:p.Glu1191Ala
|
|
|
XM_006723728.3:c.3545A>C
|
XP_006723791.1:p.Glu1182Ala
|
|
|
XM_006723730.4:c.3491A>C
|
XP_006723793.1:p.Glu1164Ala
|
|
|
XM_011528648.3:c.3836A>C
|
XP_011526950.1:p.Glu1279Ala
|
|
|
XM_011528652.2:c.3491A>C
|
XP_011526954.1:p.Glu1164Ala
|
|
|
XM_017027704.1:c.3491A>C
|
XP_016883193.1:p.Glu1164Ala
|
|
|
XM_017027705.1:c.3491A>C
|
XP_016883194.1:p.Glu1164Ala
|
|
|
XM_017027706.1:c.3422A>C
|
XP_016883195.1:p.Glu1141Ala
|
|
|
NM_015338.6:c.3575A>C
MANE Select
|
NP_056153.2:p.Glu1192Ala
|
|
