ENST00000225964.10:c.4166T>A
MANE Select
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ENSP00000225964.6:p.Leu1389His
|
|
ENST00000225964.9:c.4166T>A
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ENSP00000225964.5:p.Leu1389His
|
|
ENST00000510710.3:n.1131T>A
|
|
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NM_000088.3:c.4166T>A , LRG_1t1:c.4166T>A
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NP_000079.2:p.Leu1389His
|
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XM_005257058.3:c.3896T>A
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XP_005257115.2:p.Leu1299His
|
|
XM_005257059.3:c.3248T>A
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XP_005257116.2:p.Leu1083His
|
|
XM_011524341.1:c.3968T>A
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XP_011522643.1:p.Leu1323His
|
|
XM_005257058.4:c.3896T>A
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XP_005257115.2:p.Leu1299His
|
|
XM_005257059.4:c.3248T>A
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XP_005257116.2:p.Leu1083His
|
|
NM_000088.4:c.4166T>A
MANE Select
|
NP_000079.2:p.Leu1389His
|
|