ENST00000338034.9:c.2296C>T
MANE Select
|
ENSP00000337445.4:p.Pro766Ser
|
|
ENST00000338034.8:c.2296C>T
|
ENSP00000337445.4:p.Pro766Ser
|
|
ENST00000395962.6:c.2239C>T
|
ENSP00000379291.1:p.Pro747Ser
|
|
ENST00000426905.7:c.2176C>T
|
ENSP00000405223.3:p.Pro726Ser
|
|
ENST00000465825.5:n.2183C>T
|
|
|
ENST00000480891.5:n.2125C>T
|
|
|
ENST00000484122.5:n.3126C>T
|
|
|
ENST00000487229.6:n.1842C>T
|
|
|
ENST00000584650.5:c.1695C>T
|
|
|
NM_001165962.1:c.2176C>T
|
NP_001159434.1:p.Pro726Ser
|
|
NM_018127.6:c.2296C>T
|
NP_060597.4:p.Pro766Ser
|
|
NM_173717.1:c.2293C>T
|
NP_776065.1:p.Pro765Ser
|
|
XM_024450850.1:c.2455C>T
|
XP_024306618.1:p.Pro819Ser
|
|
XM_024450851.1:c.2377C>T
|
XP_024306619.1:p.Pro793Ser
|
|
XM_024450852.1:c.2374C>T
|
XP_024306620.1:p.Pro792Ser
|
|
XM_024450853.1:c.2371C>T
|
XP_024306621.1:p.Pro791Ser
|
|
XM_024450854.1:c.2335C>T
|
XP_024306622.1:p.Pro779Ser
|
|
XM_024450855.1:c.2254C>T
|
XP_024306623.1:p.Pro752Ser
|
|
XM_024450856.1:c.2173C>T
|
XP_024306624.1:p.Pro725Ser
|
|
XM_024450857.1:c.2173C>T
|
XP_024306625.1:p.Pro725Ser
|
|
XM_024450858.1:c.2092C>T
|
XP_024306626.1:p.Pro698Ser
|
|
XM_024450859.1:c.2089C>T
|
XP_024306627.1:p.Pro697Ser
|
|
XM_024450860.1:c.2014C>T
|
XP_024306628.1:p.Pro672Ser
|
|
XM_024450861.1:c.2014C>T
|
XP_024306629.1:p.Pro672Ser
|
|
XM_024450862.1:c.2011C>T
|
XP_024306630.1:p.Pro671Ser
|
|
NM_018127.7:c.2296C>T
MANE Select
|
NP_060597.4:p.Pro766Ser
|
|
NM_001165962.2:c.2176C>T
|
NP_001159434.1:p.Pro726Ser
|
|
NM_173717.2:c.2293C>T
|
NP_776065.1:p.Pro765Ser
|
|