ENST00000225964.10:c.1910C>T
MANE Select
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ENSP00000225964.6:p.Ala637Val
|
|
ENST00000225964.9:c.1910C>T
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ENSP00000225964.5:p.Ala637Val
|
|
ENST00000476387.1:n.259C>T
|
|
|
NM_000088.3:c.1910C>T , LRG_1t1:c.1910C>T
|
NP_000079.2:p.Ala637Val
|
|
XM_005257058.3:c.1910C>T
|
XP_005257115.2:p.Ala637Val
|
|
XM_005257059.3:c.992C>T
|
XP_005257116.2:p.Ala331Val
|
|
XM_011524341.1:c.1712C>T
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XP_011522643.1:p.Ala571Val
|
|
XM_005257058.4:c.1910C>T
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XP_005257115.2:p.Ala637Val
|
|
XM_005257059.4:c.992C>T
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XP_005257116.2:p.Ala331Val
|
|
NM_000088.4:c.1910C>T
MANE Select
|
NP_000079.2:p.Ala637Val
|
|