ENST00000225964.10:c.3125C>T
MANE Select
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ENSP00000225964.6:p.Ala1042Val
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|
ENST00000225964.9:c.3125C>T
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ENSP00000225964.5:p.Ala1042Val
|
|
ENST00000511732.1:n.69C>T
|
|
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NM_000088.3:c.3125C>T , LRG_1t1:c.3125C>T
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NP_000079.2:p.Ala1042Val
|
|
XM_005257058.3:c.2855C>T
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XP_005257115.2:p.Ala952Val
|
|
XM_005257059.3:c.2207C>T
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XP_005257116.2:p.Ala736Val
|
|
XM_011524341.1:c.2927C>T
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XP_011522643.1:p.Ala976Val
|
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XM_005257058.4:c.2855C>T
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XP_005257115.2:p.Ala952Val
|
|
XM_005257059.4:c.2207C>T
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XP_005257116.2:p.Ala736Val
|
|
NM_000088.4:c.3125C>T
MANE Select
|
NP_000079.2:p.Ala1042Val
|
|