ENST00000225964.10:c.4199C>T
MANE Select
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ENSP00000225964.6:p.Ala1400Val
|
|
ENST00000225964.9:c.4199C>T
|
ENSP00000225964.5:p.Ala1400Val
|
|
NM_000088.3:c.4199C>T , LRG_1t1:c.4199C>T
|
NP_000079.2:p.Ala1400Val
|
|
XM_005257058.3:c.3929C>T
|
XP_005257115.2:p.Ala1310Val
|
|
XM_005257059.3:c.3281C>T
|
XP_005257116.2:p.Ala1094Val
|
|
XM_011524341.1:c.4001C>T
|
XP_011522643.1:p.Ala1334Val
|
|
XM_005257058.4:c.3929C>T
|
XP_005257115.2:p.Ala1310Val
|
|
XM_005257059.4:c.3281C>T
|
XP_005257116.2:p.Ala1094Val
|
|
NM_000088.4:c.4199C>T
MANE Select
|
NP_000079.2:p.Ala1400Val
|
|