ENST00000388996.10:c.985G=
MANE Select
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ENSP00000373648.3:p.Gly329=
|
|
ENST00000521134.6:c.625G=
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ENSP00000429799.1:p.Gly209=
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|
ENST00000638588.1:c.658G=
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ENSP00000491940.1:p.Gly220=
|
|
ENST00000639358.1:c.635G=
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|
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ENST00000639496.1:c.658G=
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ENSP00000491165.1:p.Gly220=
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ENST00000388996.8:c.985G=
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ENSP00000373648.3:p.Gly329=
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|
ENST00000519445.5:c.985G=
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ENSP00000428790.1:p.Gly329=
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|
ENST00000519589.1:n.763G=
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|
|
ENST00000521134.5:c.625G=
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ENSP00000429799.1:p.Gly209=
|
|
ENST00000621976.1:c.622G=
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ENSP00000482510.1:p.Gly208=
|
|
NM_001204824.1:c.625G=
|
NP_001191753.1:p.Gly209=
|
|
NM_004519.3:c.985G=
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NP_004510.1:p.Gly329=
|
|
XM_005250914.2:c.-172G=
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XP_005250971.1:n.-172G=
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XM_006716555.2:c.277G=
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XP_006716618.1:p.Gly93=
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|
XM_011517026.1:c.625G=
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XP_011515328.1:p.Gly209=
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|
XM_005250914.3:c.-172G=
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XP_005250971.1:n.-172G=
|
|
XM_006716555.3:c.277G=
|
XP_006716618.1:p.Gly93=
|
|
XM_011517026.2:c.625G=
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XP_011515328.1:p.Gly209=
|
|
XM_017013400.1:c.763G=
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XP_016868889.1:p.Gly255=
|
|
NM_004519.4:c.985G=
MANE Select
|
NP_004510.1:p.Gly329=
|
|
NM_001204824.2:c.625G=
|
NP_001191753.1:p.Gly209=
|
|