ENST00000225964.10:c.3105C>G
MANE Select
|
ENSP00000225964.6:p.Asp1035Glu
|
|
ENST00000225964.9:c.3105C>G
|
ENSP00000225964.5:p.Asp1035Glu
|
|
ENST00000511732.1:n.49C>G
|
|
|
NM_000088.3:c.3105C>G , LRG_1t1:c.3105C>G
|
NP_000079.2:p.Asp1035Glu
|
|
XM_005257058.3:c.2835C>G
|
XP_005257115.2:p.Asp945Glu
|
|
XM_005257059.3:c.2187C>G
|
XP_005257116.2:p.Asp729Glu
|
|
XM_011524341.1:c.2907C>G
|
XP_011522643.1:p.Asp969Glu
|
|
XM_005257058.4:c.2835C>G
|
XP_005257115.2:p.Asp945Glu
|
|
XM_005257059.4:c.2187C>G
|
XP_005257116.2:p.Asp729Glu
|
|
NM_000088.4:c.3105C>G
MANE Select
|
NP_000079.2:p.Asp1035Glu
|
|