ENST00000225964.10:c.2440G>T
MANE Select
|
ENSP00000225964.6:p.Ala814Ser
|
|
ENST00000225964.9:c.2440G>T
|
ENSP00000225964.5:p.Ala814Ser
|
|
ENST00000494334.1:n.367G>T
|
|
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NM_000088.3:c.2440G>T , LRG_1t1:c.2440G>T
|
NP_000079.2:p.Ala814Ser
|
|
XM_005257058.3:c.2440G>T
|
XP_005257115.2:p.Ala814Ser
|
|
XM_005257059.3:c.1522G>T
|
XP_005257116.2:p.Ala508Ser
|
|
XM_011524341.1:c.2242G>T
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XP_011522643.1:p.Ala748Ser
|
|
XM_005257058.4:c.2440G>T
|
XP_005257115.2:p.Ala814Ser
|
|
XM_005257059.4:c.1522G>T
|
XP_005257116.2:p.Ala508Ser
|
|
NM_000088.4:c.2440G>T
MANE Select
|
NP_000079.2:p.Ala814Ser
|
|