ENST00000225964.10:c.1815C=
MANE Select
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ENSP00000225964.6:p.Gly605=
|
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ENST00000225964.9:c.1815C=
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ENSP00000225964.5:p.Gly605=
|
|
ENST00000476387.1:n.164C=
|
|
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NM_000088.3:c.1815C= , LRG_1t1:c.1815C=
|
NP_000079.2:p.Gly605=
|
|
XM_005257058.3:c.1815C=
|
XP_005257115.2:p.Gly605=
|
|
XM_005257059.3:c.958-307C=
|
XP_005257116.2:n.958-307C=
|
|
XM_011524341.1:c.1617C=
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XP_011522643.1:p.Gly539=
|
|
XM_005257058.4:c.1815C=
|
XP_005257115.2:p.Gly605=
|
|
XM_005257059.4:c.958-307C=
|
XP_005257116.2:n.958-307C=
|
|
NM_000088.4:c.1815C=
MANE Select
|
NP_000079.2:p.Gly605=
|
|