ENST00000415738.3:c.1029C>T
MANE Select
|
ENSP00000406998.2:p.Ala343=
|
|
ENST00000339711.8:c.1029C>T
|
ENSP00000339764.4:p.Ala343=
|
|
ENST00000415738.2:c.1029C>T
|
ENSP00000406998.2:p.Ala343=
|
|
ENST00000504452.5:c.1029C>T
|
ENSP00000423985.1:p.Ala343=
|
|
ENST00000515013.5:c.1029C>T
|
ENSP00000425149.1:p.Ala343=
|
|
NM_001099403.1:c.1029C>T
|
NP_001092873.1:p.Ala343=
|
|
NM_020226.3:c.1029C>T
|
NP_064611.3:p.Ala343=
|
|
XM_005263144.2:c.1032C>T
|
XP_005263201.1:p.Ala344=
|
|
XM_005263145.2:c.1032C>T
|
XP_005263202.1:p.Ala344=
|
|
XM_005263146.3:c.1029C>T
|
XP_005263203.1:p.Ala343=
|
|
XM_011532133.1:c.1872C>T
|
XP_011530435.1:p.Ala624=
|
|
XM_011532134.1:c.1869C>T
|
XP_011530436.1:p.Ala623=
|
|
XM_011532135.1:c.1731C>T
|
XP_011530437.1:p.Ala577=
|
|
XM_011532136.1:c.1584C>T
|
XP_011530438.1:p.Ala528=
|
|
XM_011532137.1:c.1584C>T
|
XP_011530439.1:p.Ala528=
|
|
XM_011532138.1:c.1584C>T
|
XP_011530440.1:p.Ala528=
|
|
XM_011532139.1:c.1584C>T
|
XP_011530441.1:p.Ala528=
|
|
XM_011532140.1:c.1584C>T
|
XP_011530442.1:p.Ala528=
|
|
XM_011532141.1:c.1446C>T
|
XP_011530443.1:p.Ala482=
|
|
XM_011532142.1:c.1425C>T
|
XP_011530444.1:p.Ala475=
|
|
XM_005263146.4:c.1029C>T
|
XP_005263203.1:p.Ala343=
|
|
XM_011532133.2:c.1872C>T
|
XP_011530435.1:p.Ala624=
|
|
XM_011532135.2:c.1731C>T
|
XP_011530437.1:p.Ala577=
|
|
XM_011532140.2:c.1584C>T
|
XP_011530442.1:p.Ala528=
|
|
XM_011532141.3:c.1446C>T
|
XP_011530443.1:p.Ala482=
|
|
XM_017008468.1:c.1581C>T
|
XP_016863957.1:p.Ala527=
|
|
XM_017008469.1:c.1668C>T
|
XP_016863958.1:p.Ala556=
|
|
XM_017008470.1:c.1584C>T
|
XP_016863959.1:p.Ala528=
|
|
NM_001099403.2:c.1029C>T
MANE Select
|
NP_001092873.1:p.Ala343=
|
|
NM_020226.4:c.1029C>T
|
NP_064611.3:p.Ala343=
|
|