ENST00000225964.10:c.1627A=
MANE Select
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ENSP00000225964.6:p.Ser543=
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|
ENST00000225964.9:c.1627A=
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ENSP00000225964.5:p.Ser543=
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|
ENST00000463440.1:n.17A=
|
|
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ENST00000471344.1:n.571A=
|
|
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NM_000088.3:c.1627A= , LRG_1t1:c.1627A=
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NP_000079.2:p.Ser543=
|
|
XM_005257058.3:c.1627A=
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XP_005257115.2:p.Ser543=
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|
XM_005257059.3:c.958-1478A=
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XP_005257116.2:n.958-1478A=
|
|
XM_011524341.1:c.1429A=
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XP_011522643.1:p.Ser477=
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|
XM_005257058.4:c.1627A=
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XP_005257115.2:p.Ser543=
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|
XM_005257059.4:c.958-1478A=
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XP_005257116.2:n.958-1478A=
|
|
NM_000088.4:c.1627A=
MANE Select
|
NP_000079.2:p.Ser543=
|
|