ENST00000338034.9:c.2333T>A
MANE Select
|
ENSP00000337445.4:p.Met778Lys
|
|
ENST00000338034.8:c.2333T>A
|
ENSP00000337445.4:p.Met778Lys
|
|
ENST00000395962.6:c.2276T>A
|
ENSP00000379291.1:p.Met759Lys
|
|
ENST00000426905.7:c.2213T>A
|
ENSP00000405223.3:p.Met738Lys
|
|
ENST00000465825.5:n.2220T>A
|
|
|
ENST00000480891.5:n.2162T>A
|
|
|
ENST00000484122.5:n.3163T>A
|
|
|
ENST00000487229.6:n.1879T>A
|
|
|
ENST00000584650.5:c.1732T>A
|
|
|
NM_001165962.1:c.2213T>A
|
NP_001159434.1:p.Met738Lys
|
|
NM_018127.6:c.2333T>A
|
NP_060597.4:p.Met778Lys
|
|
NM_173717.1:c.2330T>A
|
NP_776065.1:p.Met777Lys
|
|
XM_024450850.1:c.2492T>A
|
XP_024306618.1:p.Met831Lys
|
|
XM_024450851.1:c.2414T>A
|
XP_024306619.1:p.Met805Lys
|
|
XM_024450852.1:c.2411T>A
|
XP_024306620.1:p.Met804Lys
|
|
XM_024450853.1:c.2408T>A
|
XP_024306621.1:p.Met803Lys
|
|
XM_024450854.1:c.2372T>A
|
XP_024306622.1:p.Met791Lys
|
|
XM_024450855.1:c.2291T>A
|
XP_024306623.1:p.Met764Lys
|
|
XM_024450856.1:c.2210T>A
|
XP_024306624.1:p.Met737Lys
|
|
XM_024450857.1:c.2210T>A
|
XP_024306625.1:p.Met737Lys
|
|
XM_024450858.1:c.2129T>A
|
XP_024306626.1:p.Met710Lys
|
|
XM_024450859.1:c.2126T>A
|
XP_024306627.1:p.Met709Lys
|
|
XM_024450860.1:c.2051T>A
|
XP_024306628.1:p.Met684Lys
|
|
XM_024450861.1:c.2051T>A
|
XP_024306629.1:p.Met684Lys
|
|
XM_024450862.1:c.2048T>A
|
XP_024306630.1:p.Met683Lys
|
|
NM_018127.7:c.2333T>A
MANE Select
|
NP_060597.4:p.Met778Lys
|
|
NM_001165962.2:c.2213T>A
|
NP_001159434.1:p.Met738Lys
|
|
NM_173717.2:c.2330T>A
|
NP_776065.1:p.Met777Lys
|
|