ENST00000225964.10:c.3189T>G
MANE Select
|
ENSP00000225964.6:p.Ser1063Arg
|
|
ENST00000225964.9:c.3189T>G
|
ENSP00000225964.5:p.Ser1063Arg
|
|
ENST00000486572.1:n.7T>G
|
|
|
ENST00000511732.1:n.133T>G
|
|
|
NM_000088.3:c.3189T>G , LRG_1t1:c.3189T>G
|
NP_000079.2:p.Ser1063Arg
|
|
XM_005257058.3:c.2919T>G
|
XP_005257115.2:p.Ser973Arg
|
|
XM_005257059.3:c.2271T>G
|
XP_005257116.2:p.Ser757Arg
|
|
XM_011524341.1:c.2991T>G
|
XP_011522643.1:p.Ser997Arg
|
|
XM_005257058.4:c.2919T>G
|
XP_005257115.2:p.Ser973Arg
|
|
XM_005257059.4:c.2271T>G
|
XP_005257116.2:p.Ser757Arg
|
|
NM_000088.4:c.3189T>G
MANE Select
|
NP_000079.2:p.Ser1063Arg
|
|