ENST00000338034.9:c.2272C>T
MANE Select
|
ENSP00000337445.4:p.Pro758Ser
|
|
ENST00000338034.8:c.2272C>T
|
ENSP00000337445.4:p.Pro758Ser
|
|
ENST00000395962.6:c.2215C>T
|
ENSP00000379291.1:p.Pro739Ser
|
|
ENST00000426905.7:c.2152C>T
|
ENSP00000405223.3:p.Pro718Ser
|
|
ENST00000465825.5:n.2159C>T
|
|
|
ENST00000480891.5:n.2101C>T
|
|
|
ENST00000484122.5:n.3102C>T
|
|
|
ENST00000487229.6:n.1818C>T
|
|
|
ENST00000584650.5:c.1671C>T
|
|
|
NM_001165962.1:c.2152C>T
|
NP_001159434.1:p.Pro718Ser
|
|
NM_018127.6:c.2272C>T
|
NP_060597.4:p.Pro758Ser
|
|
NM_173717.1:c.2269C>T
|
NP_776065.1:p.Pro757Ser
|
|
XM_024450850.1:c.2431C>T
|
XP_024306618.1:p.Pro811Ser
|
|
XM_024450851.1:c.2353C>T
|
XP_024306619.1:p.Pro785Ser
|
|
XM_024450852.1:c.2350C>T
|
XP_024306620.1:p.Pro784Ser
|
|
XM_024450853.1:c.2347C>T
|
XP_024306621.1:p.Pro783Ser
|
|
XM_024450854.1:c.2311C>T
|
XP_024306622.1:p.Pro771Ser
|
|
XM_024450855.1:c.2230C>T
|
XP_024306623.1:p.Pro744Ser
|
|
XM_024450856.1:c.2149C>T
|
XP_024306624.1:p.Pro717Ser
|
|
XM_024450857.1:c.2149C>T
|
XP_024306625.1:p.Pro717Ser
|
|
XM_024450858.1:c.2068C>T
|
XP_024306626.1:p.Pro690Ser
|
|
XM_024450859.1:c.2065C>T
|
XP_024306627.1:p.Pro689Ser
|
|
XM_024450860.1:c.1990C>T
|
XP_024306628.1:p.Pro664Ser
|
|
XM_024450861.1:c.1990C>T
|
XP_024306629.1:p.Pro664Ser
|
|
XM_024450862.1:c.1987C>T
|
XP_024306630.1:p.Pro663Ser
|
|
NM_018127.7:c.2272C>T
MANE Select
|
NP_060597.4:p.Pro758Ser
|
|
NM_001165962.2:c.2152C>T
|
NP_001159434.1:p.Pro718Ser
|
|
NM_173717.2:c.2269C>T
|
NP_776065.1:p.Pro757Ser
|
|