ENST00000225964.10:c.4357G>A
MANE Select
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ENSP00000225964.6:p.Glu1453Lys
|
|
ENST00000225964.9:c.4357G>A
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ENSP00000225964.5:p.Glu1453Lys
|
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NM_000088.3:c.4357G>A , LRG_1t1:c.4357G>A
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NP_000079.2:p.Glu1453Lys
|
|
XM_005257058.3:c.4087G>A
|
XP_005257115.2:p.Glu1363Lys
|
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XM_005257059.3:c.3439G>A
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XP_005257116.2:p.Glu1147Lys
|
|
XM_011524341.1:c.4159G>A
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XP_011522643.1:p.Glu1387Lys
|
|
XM_005257058.4:c.4087G>A
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XP_005257115.2:p.Glu1363Lys
|
|
XM_005257059.4:c.3439G>A
|
XP_005257116.2:p.Glu1147Lys
|
|
NM_000088.4:c.4357G>A
MANE Select
|
NP_000079.2:p.Glu1453Lys
|
|