ENST00000225964.10:c.4361T>G
MANE Select
|
ENSP00000225964.6:p.Phe1454Cys
|
|
ENST00000225964.9:c.4361T>G
|
ENSP00000225964.5:p.Phe1454Cys
|
|
NM_000088.3:c.4361T>G , LRG_1t1:c.4361T>G
|
NP_000079.2:p.Phe1454Cys
|
|
XM_005257058.3:c.4091T>G
|
XP_005257115.2:p.Phe1364Cys
|
|
XM_005257059.3:c.3443T>G
|
XP_005257116.2:p.Phe1148Cys
|
|
XM_011524341.1:c.4163T>G
|
XP_011522643.1:p.Phe1388Cys
|
|
XM_005257058.4:c.4091T>G
|
XP_005257115.2:p.Phe1364Cys
|
|
XM_005257059.4:c.3443T>G
|
XP_005257116.2:p.Phe1148Cys
|
|
NM_000088.4:c.4361T>G
MANE Select
|
NP_000079.2:p.Phe1454Cys
|
|