ENST00000262367.10:c.5443G=
MANE Select
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ENSP00000262367.5:p.Gly1815=
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ENST00000262367.9:c.5443G=
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ENSP00000262367.5:p.Gly1815=
|
|
ENST00000382070.7:c.5329G=
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ENSP00000371502.3:p.Gly1777=
|
|
NM_001079846.1:c.5329G=
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NP_001073315.1:p.Gly1777=
|
|
NM_004380.2:c.5443G=
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NP_004371.2:p.Gly1815=
|
|
XM_005255124.3:c.5398G=
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XP_005255181.1:p.Gly1800=
|
|
XM_005255125.3:c.5026G=
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XP_005255182.1:p.Gly1676=
|
|
XM_006720848.2:c.5182G=
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XP_006720911.1:p.Gly1728=
|
|
XM_011522380.1:c.5389G=
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XP_011520682.1:p.Gly1797=
|
|
XM_011522381.1:c.4690G=
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XP_011520683.1:p.Gly1564=
|
|
XM_005255124.4:c.5398G=
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XP_005255181.1:p.Gly1800=
|
|
XM_005255125.4:c.5026G=
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XP_005255182.1:p.Gly1676=
|
|
XM_006720848.3:c.5182G=
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XP_006720911.1:p.Gly1728=
|
|
XM_011522381.2:c.4690G=
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XP_011520683.1:p.Gly1564=
|
|
XM_017022944.1:c.5437G=
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XP_016878433.1:p.Gly1813=
|
|
NM_004380.3:c.5443G=
MANE Select
|
NP_004371.2:p.Gly1815=
|
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