ENST00000388996.10:c.984A>G
MANE Select
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ENSP00000373648.3:p.Glu328=
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ENST00000521134.6:c.624A>G
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ENSP00000429799.1:p.Glu208=
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ENST00000638588.1:c.657A>G
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ENSP00000491940.1:p.Glu219=
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ENST00000639358.1:c.634A>G
|
|
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ENST00000639496.1:c.657A>G
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ENSP00000491165.1:p.Glu219=
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ENST00000388996.8:c.984A>G
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ENSP00000373648.3:p.Glu328=
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ENST00000519445.5:c.984A>G
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ENSP00000428790.1:p.Glu328=
|
|
ENST00000519589.1:n.762A>G
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|
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ENST00000521134.5:c.624A>G
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ENSP00000429799.1:p.Glu208=
|
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ENST00000621976.1:c.621A>G
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ENSP00000482510.1:p.Glu207=
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|
NM_001204824.1:c.624A>G
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NP_001191753.1:p.Glu208=
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|
NM_004519.3:c.984A>G
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NP_004510.1:p.Glu328=
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XM_005250914.2:c.-173A>G
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XP_005250971.1:n.-173A>G
|
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XM_006716555.2:c.276A>G
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XP_006716618.1:p.Glu92=
|
|
XM_011517026.1:c.624A>G
|
XP_011515328.1:p.Glu208=
|
|
XM_005250914.3:c.-173A>G
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XP_005250971.1:n.-173A>G
|
|
XM_006716555.3:c.276A>G
|
XP_006716618.1:p.Glu92=
|
|
XM_011517026.2:c.624A>G
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XP_011515328.1:p.Glu208=
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XM_017013400.1:c.762A>G
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XP_016868889.1:p.Glu254=
|
|
NM_004519.4:c.984A>G
MANE Select
|
NP_004510.1:p.Glu328=
|
|
NM_001204824.2:c.624A>G
|
NP_001191753.1:p.Glu208=
|
|