ENST00000225964.10:c.4175G=
MANE Select
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ENSP00000225964.6:p.Gly1392=
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ENST00000225964.9:c.4175G=
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ENSP00000225964.5:p.Gly1392=
|
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ENST00000510710.3:n.1140G=
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|
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NM_000088.3:c.4175G= , LRG_1t1:c.4175G=
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NP_000079.2:p.Gly1392=
|
|
XM_005257058.3:c.3905G=
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XP_005257115.2:p.Gly1302=
|
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XM_005257059.3:c.3257G=
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XP_005257116.2:p.Gly1086=
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XM_011524341.1:c.3977G=
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XP_011522643.1:p.Gly1326=
|
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XM_005257058.4:c.3905G=
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XP_005257115.2:p.Gly1302=
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XM_005257059.4:c.3257G=
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XP_005257116.2:p.Gly1086=
|
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NM_000088.4:c.4175G=
MANE Select
|
NP_000079.2:p.Gly1392=
|
|